Catalogue
Transcription
Catalogue
Catalogue Catalogue Chemical Reference Substances Infrared Reference Spectra Biological Reference Preparations List No. 48 December 2006 © European Pharmacopoeia - Catalogue, December 2006 i Catalogue I. TERMS OF SUPPLY All items listed in this catalogue are supplied strictly on the basis of these Terms of Supply, whose provisions shall have effect notwithstanding any inconsistent provision contained in any document received from a purchaser. 1. Quality and purpose of items supplied All chemical substances or biological preparations listed in this catalogue are supplied exclusively as European Pharmacopoeia Chemical Reference Substances, Biological Reference Preparations or Reference Spectra (Ph. Eur. CRS, BRP or RS) for use as reference standards in tests and assays carried out in accordance with the official methods of the European Pharmacopoeia (Ph. Eur.) and for no other purpose. The Council of Europe accordingly makes no representation, contractual statement, or expression of opinion concerning the quality or safety of any item supplied, the presence of any defect in it, or its fitness for any particular purpose except that of use as a Ph. Eur. CRS, BRP or RS in tests and assays carried out in accordance with the official methods of the Ph. Eur. by professional persons having technical skill and at their own discretion and risk. It is for the purchasers of any such item who are responsible for persons in a workplace to determine independently the risks associated with the item according to the conditions of use and to take appropriate safety measures, including provision of appropriate information to persons working with the substance. Any liability of the Council of Europe for injury, loss or damage arising from the supply or use of any such item is in any event hereby excluded to the fullest extent permitted by law; in particular, no liability is accepted for loss of profits or indirect or consequential loss. 2. Prices 2.1. PRICE LIST Prices are identified for each product in the list starting on page 1. However, please note that prices and package sizes are subject to change without notice. The European Directorate for the Quality of Medicines (EDQM) does not operate a discount policy. The sale prices are exclusive of duties and taxes and are given in Euros. It is the responsibility of the buyer (or the recipient of the delivery if different from the buyer) to contact the national fiscal or customs authorities to pay the duties and taxes. In no event shall the said duties and taxes be paid by the Council of Europe (EDQM). In the European Union (EU), there is no VAT identification number for organisations with diplomatic status. The Council of Europe (EDQM) therefore has no VAT identification number and is not subject to duties and taxes. The goods remain the property of the Council of Europe (EDQM) until the invoice has been paid in full. Catalogue items are not returnable for exchange or refund. 2.2. DELIVERY AND RELATED COSTS on a DDU (Incoterms 2000) basis, namely, delivered duty unpaid insurance included. Where the shipment is identified below as airport consignment (see section Delivery charges), the goods are shipped to the buyer on a CIP (Incoterms 2000) basis, namely carriage and insurance included. — The Council of Europe (EDQM) delivers the goods to the buyer not cleared for import and not unloaded by any means of transport. — The Council of Europe (EDQM) bears the cost and risks of packing, transport to the delivery site and insurance. — In no event shall the Council of Europe (EDQM) be held responsible for any deterioration of the goods due to their delayed delivery by the carrier. — The buyer is responsible for the cost of import customs clearance, for paying the duties and taxes required in the country of import and for unloading the goods. Where the shipping costs are paid by the customer, the goods are shipped to the buyer on an EX Works (Incoterms 2000) basis, with neither carriage nor insurance included. Therefore, the Council of Europe (EDQM) takes no responsibility in any case of deterioration or loss of goods. — The buyer shall be entirely responsible if the goods are held up at customs at the time of import into the buyer’s country. In no event shall the Council of Europe (EDQM) be able to provide any assistance. Delivery charges The extra charges are applied per shipment. A shipment comprises only the reference standards that can be shipped under the same conditions. Consequently, goods requiring specific packaging (eg ice, dry-ice), dangerous goods or controlled substances will be invoiced separately from the rest of the order and extra charges will be incurred. As one order could include several shipments, the Council of Europe (EDQM) advises its customers to re-group their orders by type of shipment so the customers can better track the progress of a complete order and to save money in shipping charges. Where the buyer requests shipping conditions other than those recommended in our catalogue, or another carrier, the Council of Europe (EDQM) takes no responsibility in any case of deterioration of the goods or loss of parcel. Extra charges (postage and packaging) will be applied in the following cases. Please note that prices are subject to change without notice. a) Shipment at ambient temperature — France: no extra charge, price is inclusive of packaging and postage. At the client’s request, express courier delivery is charged at 18 EUR per shipment — EU: 18 EUR per shipment — Other European countries: 80 EUR per shipment — Outside Europe: 120 EUR per shipment (Note: for India, South America and Africa, our shipment is by airport consignment only) Unless otherwise stated below or specifically agreed with the customer, the goods are shipped to the buyer — Shipping costs paid by the customer: 10 EUR per shipment ii © European Pharmacopoeia - Catalogue, December 2006 Catalogue b) Shipment under ice (+ 5 °C): sent in cooled freight containers, either by express courier or by airfreight (Note: for all countries inside the EU (with the exception of Cyprus) our shipment is on a ‘door to door’ basis. For all other countries (and the exceptions above), our shipment is by airport consignment only) — EU: 50 EUR per shipment — Other European countries: 70 EUR per shipment — Outside Europe: 120 EUR per shipment — Shipping costs paid by the customer: 20 EUR per shipment c) Shipment under ice (- 20 °C): sent in cooled freight containers, either by express courier or by airfreight g) Dangerous goods in excepted quantities: sent by carrier chosen by EDQM (Note: for countries inside the EU (with the exception of Cyprus and Malta), our shipment is on a ‘door to door’ basis. For all other countries (and the exceptions above), our shipment is by airport consignment only, and an express courier delivery cannot be used.) — EU: 50 EUR per shipment — Other European countries: 125 EUR per shipment — Outside Europe: 125 EUR per shipment h) Dangerous goods sent by road: carrier chosen by EDQM — EU: 150 EUR per item (‘door to door’) — Other European countries: 180 EUR per item (‘door (Note: for all countries inside the EU (with the to door’) exception of Cyprus) our shipment is on a ‘door to door’ basis. For all other countries (and the exceptions — Outside Europe: cannot be sent above), our shipment is by airport consignment only) i) Precursors (controlled drugs: sent by carrier chosen — EU: 50 EUR per shipment by EDQM) — Other European countries: 70 EUR per shipment — Outside Europe: 120 EUR per shipment — Shipping costs paid by the customer: 20 EUR per shipment d) Shipment under dry-ice: sent in cooled freight containers (dry-ice), either by express courier or by airfreight (Note: for all countries inside the EU (with the exception of Cyprus and Malta) our shipment is on a ‘door to door’ basis. For all other countries (and the exceptions above), our shipment is by airport consignment only) — EU: 90 EUR per shipment — Other European countries: 120 EUR per shipment — Outside Europe: 200 EUR per shipment — Shipping costs paid by the customer: 55 EUR per shipment e) Hepatitis C virus BRP, B19 virus DNA for NAT: dry ice + dangerous goods – from 5 to 100 vials (from 1 to 20 sales units), sent by carrier chosen by EDQM. For orders of over 100 vials (20 sales units): prices on request (Note: for countries outside France, our shipment is by airport consignment only) — EU: 250 EUR per shipment (Note for countries outside the EU, our shipment is by airport consignment only) — France: no extra charge, price is inclusive of packaging and postage. At the client’s request, express courier delivery is charged at 18 EUR per shipment — EU: 18 EUR per shipment — Other European countries: 160 EUR per shipment — Outside Europe: 160 EUR per shipment NB: these extra charges include packaging, shipping and management of permits j) Psychotropic substances (controlled drugs: sent by carrier chosen by EDQM) (Note for countries outside France, our shipment is by airport consignment only) — France: no extra charge, price is inclusive of packaging and postage. At the client’s request, express courier delivery is charged at 18 EUR per shipment — EU (except France): 110 EUR per shipment — Outside EU: 160 EUR per shipment NB: these extra charges include packaging, shipping and management of permits k) Narcotics (controlled drugs: sent by carrier chosen by EDQM) (Note for countries outside France, our shipment is by airport consignment only) — Other European countries: 250 EUR per shipment — France: 50 EUR per shipment — Outside Europe: 250 EUR per shipment — EU (except France): 110 EUR per shipment f) Dangerous goods: sent by airfreight chosen by EDQM — Outside EU: 160 EUR per shipment (Note: for countries outside France, our shipment is by airport consignment only) NB: these extra charges include packaging, shipping and management of permits — EU: 150 EUR per item l) Reference spectra — Other European countries: 180 EUR per item — France: no extra charge, price is inclusive of packaging and postage. At the client’s request, express courier delivery is charged at 18 EUR per shipment — Outside Europe: 250 EUR per item © European Pharmacopoeia - Catalogue, December 2006 iii Catalogue — EU: 18 EUR per shipment — Other countries: 50 EUR per shipment — Shipping costs paid by the customer: 10 EUR per shipment 3. How do I order? The reference standards are supplied by the EDQM. 3.1. ORDER FORM Please send your order using the CRS order form (see page xv of this catalogue) or by sending an official purchase order on company letterhead to the EDQM. The order form may be downloaded from www.pheur.org under Reference Standards (Ph. Eur. Reference Standards). Fax: +33 (0)3 88 41 27 71 for the attention of Sales Section E-mail: [email protected] Letter: Council of Europe, European Directorate for the Quality of Medicines, Sales Section, 7 allée Kastner, CS 30026, F-67081 Strasbourg, France Unfortunately, we will not be able to process any orders received without the above information. 3.2. QUANTITIES A Reference Standard may include several vials/ampoules (see Sales unit in the catalogue). In such instances do not order in terms of the total number of vials/ampoules but in sales units. Example: to obtain 4 vials of Calcitonin, you have to order: Reference C0200000, Quantity 2. It is the policy of EDQM to limit the purchase quantities of the same reference standards where stock levels are low. The EDQM will do everything possible to ensure all orders are dispatched in their entirety, but when quantities of CRSs or BRPs are limited, the EDQM will try to dispatch orders in such a way that as many customers as possible will receive at least some of the limited quantities. 3.3. SPECIAL DOCUMENTATION 3.3.1. For all products It is the responsibility of the customer to check if a Customers are financially responsible for duplicate orders special permit is needed in the importing country for the in the following cases: given product or if, for the given product, no importation at all is allowed. All necessary documentation has to be — confirmation orders that are not clearly marked as provided with the order (especially as regards biological being a confirmation of an order that has already products). For customers in China: an additional form been sent to the Council of Europe (EDQM) has to be completed and to accompany each Reference — submission of the same order multiple times (i.e., via Standard order (see example on page xix of this fax, e-mail, mail or any combination thereof) catalogue). Please note that we do not accept orders by telephone. 3.3.2. Controlled drugs If you are using any other documentation other than the official CRS order form please ensure you have included: — 3.3.2.1. Psychotropic substances and narcotics of the Vienna Convention — details of the Invoicing/Billing address including name of company, post code, town, country and telephone number As our premises are located in France, the reference to “*psy” and “*narc” given in the catalogue, only refers to the French legislation. — details of the Delivery/Dispatch address (if different) including name of company, post code, town, country (please note STREET ADDRESS ONLY, no P.O. Boxes) France: to order a psychotropic substance, the form has to be sent exclusively by mail, with the appropriate licence to hold such a substance. — contact name, telephone number, fax number and e-mail address: an e-mail address is required for order confirmation and shipping notification purposes — VAT number (mandatory within the European Union) — your order reference/purchase order reference — item order code — official name of the Reference Standard as set out in this catalogue — sales/unit quantity — name and account number of the carrier (if you wish to use your own) If orders are received without the official name of the Reference Standard and the full item order code (as set out in the catalogue) the EDQM takes no responsibility for an incorrect item being dispatched. iv Other countries: to order a psychotropic substance, the form has to be sent exclusively by mail. These substances are subject to import and export control in certain countries. It is the responsibility of the customer to obtain any necessary documents to comply with the laws of the importing country. An import permit (in French or with a certified French translation attached) must be valid for at least 6 months from the date of its receipt by the Council of Europe (EDQM). — 3.3.2.2. Chemical precursors of narcotics (Vienna Convention) Countries from the EU: the order of a substance(s) frequently used for the illegal production of narcotics and psychotropic substances (reference “*Drug precursor” in the catalogue) has to be accompanied by the end user declaration form stating the use(s) of the substance(s) in line with the current European form (see example on page xvii of the catalogue). © European Pharmacopoeia - Catalogue, December 2006 Catalogue Other countries: it is the responsibility of the customer to obtain any necessary documents to comply with the laws of the importing country. An import permit (in French or with a certified French translation attached) must be valid for at least 6 months from the date of its receipt by the Council of Europe (EDQM). Special charges are required (see 2.2.h and 2.2.i). For certain countries, especially those having strict monetary regulations, new clients and large orders, we reserve the right to require pre-payment. In case of doubt, please contact us at [email protected]. Payment by letter of credit is not accepted. 5. Regulatory procedures and SH/NDP (harmonised system – nomenclature for customs clearance of goods) Export permits for psychotropic drugs and precursors In the event of special requirements in the buyer’s country, the buyer shall obtain the import authorisations are required before the goods can be dispatched. and resolve any regulatory matters before the goods 3.4. ORDER PROCESSING AND INVOICING are ordered and shipped. The buyer shall be entirely responsible if the goods are held up at customs at the On receiving the completed order, the EDQM aims to time of import into the buyer’s country. In no event shall invoice and dispatch all orders within 2-3 working days the Council of Europe (EDQM) be able to provide any with the exception of: assistance. — orders for controlled drugs, Origin of the goods: Diplomatic, Council of EuropeFrance. — shipments to be made under ice (these are dispatched only on Mondays and Tuesdays) SH/NDP 000009. or dry-ice (these are dispatched only on Mondays), The SH/NDP is strictly limited to export operations out of — orders where pre-payment is required. France. Please note : The importer shall be personally responsible for the tariff classification in the country of import and will — For all customers from the EU, except France, all assume the ensuing regulatory, fiscal, health and safety psychotropic drugs will be invoiced separately from obligations. the rest of your order and extra charges will be incurred (see 2.2.h). 6. Complaints — For all customers outside the EU, all psychotropic Complaints related to delivery drugs and precursors will be invoiced separately from Any delays in delivery do not entitle the buyer to cancel the rest of your order and in all cases extra charges the sale, refuse the goods or claim damages. will be incurred (see 2.2.h and 2.2.i). Complaints can be made by the buyer upon delivery of — For all customers from the EU, all orders for goods only if the goods do not correspond quantitatively precursors need to be accompanied by the valid or qualitatively (if the package containing the goods is End User Declaration. The End User Declaration for precursors is included on page xvii of this catalogue. badly damaged). Complaints must be made to the carrier in writing at the Delays in shipping will occur if all documentation time of delivery. is not available when your order is placed. For this reason we kindly ask customers to order controlled A copy of the complaints must be sent to the Council of drugs separately from other reference standards. Europe (EDQM) (by e-mail or fax) no later than 12 hours after the complaints were made. 4. Payment Payment can be made by cheque made payable to the Council of Europe/EDQM and be sent to the above address (see 3.1) or by bank transfer. Société Générale, 255, route de Mittelhausbergen, 67200 Strasbourg, France IBAN Account Number for International Transfers: (FR 76) 30003 02360 00550034256 76 National transfers: 30003 02360 00550034256 76 SWIFT: SOGEFRPP You can also pay by credit card (Visa, Eurocard, Mastercard or American Express) by writing down the card number, the expiry date, the card holder’s name and not forgetting the card holder’s signature. Please note that we do not accept credit card numbers by telephone. In all cases, the payment should be net of charge for the Council of Europe and invoices should be paid within 30 days from the date of invoice. Any other fees, such as customs duties, taxes, or tariffs are also the responsibility of the customer. © European Pharmacopoeia - Catalogue, December 2006 Complaints related to the order Complaints can be made by the buyer upon delivery of goods only if the goods do not correspond quantitatively with the initial order. Any complaints should be sent within 48 hours of the time of delivery of the goods in the original package. For airport deliveries, any complaint should be sent within a week of the time of delivery at the airport. If the complaint made at the time of delivery is shown to be justified because the package and the goods are badly damaged or because an error clearly has been made, the Council of Europe (EDQM) will be free to choose between issuing a credit note, refunding the customer or making another delivery of similar goods. In the event of complaints, shipping costs and other costs (customs) to return goods to the Council of Europe (EDQM) will be borne by the buyer. In no event shall the customer return goods to the Council of Europe (EDQM) unless the Council of Europe v Catalogue (EDQM) has been notified and has given its written consent. II. EDQM LONG-TERM STORAGE CONDITIONS We will not accept or exchange any returned goods unless See the relevant column in the list starting on page 1. the customer complies with the terms and conditions and the above procedure. 7. Responsibility The Council of Europe (EDQM) cannot be held responsible for failure to meet the requirements of the legislation of the country where the goods are delivered. It is the customer’s responsibility to check with the local authorities to make sure that the goods or services that they intend to order can be imported or used in that country. III. IDENTIFICATION OF REFERENCE STANDARDS The names of the reference standards printed in this catalogue are those used in the official monographs of the Ph. Eur. (English version) in alphabetical order (name in italics followed by CRS or BRP). IV. USE OF REFERENCE The customer is solely responsible for the choice of STANDARDS products, their storage from the time of delivery and their use. In no event shall the Council of Europe (EDQM) be The reference standards of the Ph. Eur. are established liable for any consequent damage. and distributed following the general principle of ISO The Council of Europe (EDQM) guarantees that the goods standard 34. have been submitted to the carrier in perfect condition. The specificity of pharmacopoeial reference standards This is the only guarantee given by the Council of has been officially recognised in the introduction of the Europe (EDQM). No other guarantees, whether express revision of ISO standard ISO 34 - General requirements or implied, are given by the Council of Europe (EDQM). for the competence of reference material producers In particular, the Council of Europe (EDQM) does not (Second Edition 2000): “Pharmacopoeial standards guarantee that the goods will meet the customer’s and substances are established and distributed by specific expectations. pharmacopoeial authorities following the general The Council of Europe (EDQM) cannot be held responsible for the contract not being fulfilled in the event of goods being out of stock or unavailable, force majeure, disturbances or total or partial strike action affecting in particular postal services and means of transport, and flood or fire. 8. Disputes In accordance with the provisions of article 21 of the General Agreement on the Privileges and Immunities of the Council of Europe, all disputes between the Council of Europe (EDQM) and the customer as regards the application of this contract shall be submitted, if a mutual agreement cannot be reached between the parties, to arbitration as laid down in Order No. 481 of the Secretary General, approved by the Committee of Ministers. Answers to Your Questions Reference Standards - Questions about orders, billing, and shipping information. Helpdesk: http://www.pheur.org/hd Fax: +33 (0)3 88 41 27 71 Flight details - Questions about dispatch of CRS orders only. Helpdesk: http://www.pheur.org/hd E-mail: [email protected] Fax: +33 (0)3 88 41 27 71 principle of this guide. It should be noted, however, that a different approach is used by the pharmacopoeial authorities to give the user the information provided by certificate of analysis and the expiration dates. Also, the uncertainty of their assigned values is not stated since it is negligible in relation to the defined limits of the method-specific assays of the pharmacopoeias for which they are used.” The reference standards are specially selected and verified batches, suitable for use as prescribed in the Pharmacopoeia. The column ‘Monograph’ lists the monograph(s) and/or general method(s) of analysis for which the reference standard is intended. The monograph number requires four digits (for example monograph 0076), a general chapter requires five digits (for example the text 5.4 is indicated with the number 50400, the method 2.5.1 is indicated with the number 20501). These numbers are available on the top of the monograph, and correspond to the identification number of the document. Suitability for purposes other than those prescribed in the Ph. Eur. monographs is left up to the user. Each vial supplied contains a quantity sufficient for the prescribed use. A vial or an ampoule is considered as an ‘immediate use’ reference standard. It is recommended that the vial or ampoule is used in the same series of analysis. Monographs - Questions about monographs It is recommended to purchase only a sufficient amount for immediate use and to use the reference standards as soon as possible. Helpdesk: http://www.pheur.org/hd Fax: +33 (0)3 88 41 27 71 The stability of the contents of opened vials or ampoules cannot be guaranteed. An electronic version of the Reference Standards Catalogue (using Adobe Acrobat version 5) and other information is available on our website www.pheur.org In specific cases, for reasons related to filling or labelling, sub-batches 1.1, 1.2, 1.3, etc., are obtained from the same batch of bulk material. (Note: the previous classification vi © European Pharmacopoeia - Catalogue, December 2006 Catalogue of the sub-batches 1a, 1b, 1c, will be gradually replaced with 1.1, 1.2, 1.3, etc.) provided with the previous batch. An example of a BVS is included on pages xx and xxi of this catalogue. However, all necessary precautions are taken in order to guarantee that the quality and the specifications of the sub-batches do not differ from one to another. For reference standards supplied in sealed glass ampoules the following technique is suitable for opening the ampoule: tap the ampoule gently to collect the material at the lower end; score the ampoule with a file; heat a glass rod to white heat and apply firmly to the file mark; if a crack is not produced, deepen and extend the file mark, reheat the glass rod and apply again. Since CRSs and BRPs are officially certified by the European Pharmacopoeia Commission, which adopts the reports establishing their suitability for the intended use, it should be noted that neither certificates of analysis nor data not relevant to the use of the products as defined by the Ph. Eur. monograph are provided with the reference standard. In the same way, no expiry date is indicated because the reference standards comply with the requirements of the corresponding monograph and are monitored regularly. The ‘Information’ column of the catalogue indicates an official date on which the batch is no longer valid as a CRS/BRP for all batches that have just been replaced. Hence “batch 1 valid until 30 June 2006” means that batch 1 is no longer official as of 1 July 2006. Toxic substances. The potential toxicity of certain reference standards is such that special precautions are needed during use to avoid contact. Such substances should be manipulated in a glove box, otherwise protective gloves, eye protection and a mask should be worn. Biological preparations and blood products. These preparations should be regarded as potentially hazardous to health and should be used and disposed of according to your own Laboratory safety practices. Safety Data Sheets Where no drying conditions are stated, the substance is to be used as received. For the CRS with an assigned content, the stated content is expressed on an ‘as is’ basis. The reference standards database on our website is now updated daily with information on availability. Other information available includes details on the origin, assigned value and batch validity. A batch validity statement (BVS) for the reference standards is now available. It enables the user of a reference standard to print a validity statement directly from the reference standards database on the EDQM website (http://crs.pheur.org/). This tool will help users to assure the traceability of validity dates and leaflets © European Pharmacopoeia - Catalogue, December 2006 Safety data sheets are available on the website or on request. Information provided by the Ph. Eur. on the safety data sheets is compiled from information provided in the usual way by suppliers or manufacturers of the products and has not been independently verified by Ph. Eur. staff. The accuracy of such information cannot therefore be guaranteed. V. LEAFLET In specific cases, an explanatory leaflet is sent with the product. See the relevant column in the list starting on page 1 (where nothing is stated, no leaflet is needed for the given product). Leaflets are also available on the website. vii Catalogue I. CONDITIONS GÉNÉRALES La fourniture des articles contenus dans le présent catalogue est effectuée conformément aux termes des Conditions Générales : les dispositions des Conditions Générales s’appliquent, nonobstant toute disposition contraire contenue dans tout document reçu d’un acquéreur. 1. Qualité et usage des articles fournis Toute substance chimique ou toute préparation biologique inscrite dans ce catalogue est exclusivement fournie au titre, soit de Substance Chimique de Référence, soit de Préparation Biologique de Référence, ou bien encore de Spectre de Référence de la Pharmacopée Européenne (SCR, PBR, SR Ph. Eur.). Ces produits sont utilisés en tant qu’étalons de référence dans les essais et les dosages réalisés conformément aux prescriptions des méthodes officielles de la Pharmacopée Européenne (Ph. Eur.) et à aucune autre fin. Les produits demeurent la propriété du Conseil de l’Europe (DEQM) jusqu’au complet paiement de la facture. Les produits ne sont ni échangés ni repris. 2.2. LIVRAISON ET SUPPLÉMENTS SPÉCIAUX Sauf accord particulier, la livraison des produits est réalisée en DDU (Incoterms 2000) à l’acheteur, c’est-àdire en « rendu droits et taxes non acquittés assurance incluse». Pour les envois en rendu aéroport (voir section Frais de livraison), la livraison des produits est réalisée en CIP (Incoterms 2000) à l’acheteur, c’est-à-dire en « port payé assurance incluse». — Le Conseil de l’Europe (DEQM) livre à l’acheteur le produit non dédouané à l’importation et non déchargé à l’arrivée de tout véhicule de transport. — Le Conseil de l’Europe (DEQM) supporte les frais et risques liés à l’emballage, le transport jusqu’au lieu de livraison et l’assurance. — Il s’ensuit que le Conseil de l’Europe n’émet aucun avis, ne fait aucune déclaration et n’assume aucune garantie concernant la qualité ou la sécurité des articles fournis, l’absence d’un quelconque défaut ou leur aptitude à toute autre fin, excepté dans le cadre de leur usage au — titre de SCR, PBR, SR Ph. Eur. dans les essais et dosages réalisés conformément aux prescriptions des méthodes officielles de la Ph. Eur. par des personnes spécialisées disposant d’une compétence technique, et à leurs risques et périls. Il appartient aux acquéreurs de tels articles, qui sont responsables des personnes à leur poste de travail, de vérifier, à titre personnel, les risques inhérents à l’article selon les conditions d’utilisation et de prendre les mesures de sécurité appropriées à l’égard des personnes travaillant avec la substance. Le Conseil de l’Europe décline, dans les limites autorisées par la loi, toute responsabilité à l’égard de tout dommage, de tout sinistre ou de tout préjudice liés à la fourniture ou à l’utilisation — d’un tel article. Le Conseil de l’Europe n’assume notamment aucune responsabilité relative au manque à gagner ou à toute autre perte indirecte. 2. Prix 2.1. LISTE DES PRIX Les prix sont indiqués pour chaque produit dans la liste débutant page 1. Toutefois, veuillez noter que les prix et les quantités unitaires peuvent changer sans préavis. La Direction Européenne de la Qualité du Médicament (DEQM) ne pratique pas de politique de remise de prix. Les prix s’entendent hors droits et taxes. Ils sont indiqués en euros. Il appartient à l’acheteur (ou le preneur s’il est différent de l’acheteur) de contacter, selon son statut, son autorité fiscale ou douanière nationale pour le paiement des droits et des taxes dont il serait redevable au titre de la présente commande. Lesdits droits et taxes ne pourront être pris en charge par le Conseil de l’Europe (DEQM) en aucune façon. Dans l’Union Européenne (UE), le régime diplomatique ne possède pas de numéro d’identification TVA. Aussi, le Conseil de l’Europe (DEQM) n’a pas de numéro d’identification TVA et est un non-assujetti exonéré de droits et de taxes. viii En aucun cas, le Conseil de l’Europe (DEQM) ne saurait être responsable d’une éventuelle détérioration des produits du fait de leur retrait tardif auprès du transporteur. Restent à la charge de l’acheteur : les frais des formalités d’importation et de mise à la consommation, les droits et les taxes dont il serait redevable dans son pays, le déchargement de la marchandise. Quand les coûts d’expédition sont à la charge de l’acheteur, la livraison des produits est réalisée en EX Works (Incoterm 2000) à l’acheteur, ni les frais de port, ni l’assurance ne sont inclus. Par conséquent, le Conseil de l’Europe (DEQM) ne saurait être tenu pour responsable en cas de détérioration des produits ou de perte du paquet. En cas de blocage douanier au moment de l’importation dans le pays de l’acheteur, ce dernier assumera la responsabilité pleine et entière. Le Conseil de l’Europe (DEQM) ne pourra en aucun cas intervenir dans une quelconque assistance. Frais de livraison Un supplément spécial est ajouté par envoi. Un envoi comprend uniquement les étalons de référence qui peuvent être expédiés dans les mêmes conditions. Ainsi, les produits nécessitant un emballage particulier (glace, carboglace), les produits dangereux ou les substances contrôlées seront facturés séparément du reste de la commande, et les suppléments spéciaux seront ajoutés. Comme une commande peut faire l’objet de plusieurs envois, le Conseil de l’Europe (DEQM) conseille à ses clients de regrouper leurs commandes en fonction du type d’envoi, ainsi les clients pourront mieux suivre la progression de leur commande complète et économiser des frais d’expédition. Si un acheteur demande des conditions d’envois autres que celles recommandées dans notre catalogue, ou un autre transporteur, le Conseil de l’Europe (DEQM) ne saurait être tenu responsable en cas de détérioration des produits ou de perte du paquet. Un supplément spécial (emballage et expédition) est demandé dans les cas suivants. Veuillez noter que les prix peuvent changer sans préavis. © European Pharmacopoeia - Catalogue, December 2006 Catalogue a) Envoi à température ambiante — UE : 250 EUR par envoi — France : pas de supplément spécial, le prix s’entend emballage et expédition par la poste compris. Sur demande du client, un envoi express est facturé 18 EUR par envoi — Autres pays d’Europe : 250 EUR par envoi — UE : 18 EUR par envoi — Autres pays d’Europe : 80 EUR par envoi — Hors Europe : 250 EUR par envoi f) Marchandises dangereuses : expédiées par un transitaire choisi par la DEQM (Pour les pays hors France, la livraison est en rendu aéroport uniquement) — Hors Europe : 120 EUR par envoi (Pour l’Inde, l’Amérique du Sud et l’Afrique, la livraison est en rendu aéroport uniquement) — UE : 150 EUR par article — Coûts d’expédition à la charge de l’acheteur : 10 EUR par envoi — Hors Europe : 250 EUR par article b) Envoi sous glace (+ 5 °C) : expédiés par express ou par transitaire, en conteneurs réfrigérés g) Matières dangereuses en quantités exemptées : expédiées par un transporteur choisi par la DEQM (Pour tous les pays de l’UE (à l’exception de Chypre) la livraison est en rendu domicile. Pour ces derniers et tous les autres, la livraison est en rendu aéroport uniquement) — UE : 50 EUR par envoi — Autres pays d’Europe : 70 EUR par envoi — Hors Europe : 120 EUR par envoi — Coûts d’expédition à la charge de l’acheteur : 20 EUR par envoi c) Envoi sous glace (- 20 °C) : expédiés par express ou par transitaire, en conteneurs réfrigérés (Pour tous les pays de l’UE (à l’exception de Chypre) la livraison est en rendu domicile. Pour ces derniers et tous les autres, la livraison est en rendu aéroport uniquement) — UE : 50 EUR par envoi — Autres pays d’Europe : 70 EUR par envoi — Hors Europe : 120 EUR par envoi — Coûts d’expédition à la charge de l’acheteur : 20 EUR par envoi d) Envoi sous carboglace : par express ou par transitaire, en conteneurs réfrigérés (Pour tous les pays de l’UE (à l’exception de Chypre et Malte) la livraison est en rendu domicile. Pour ces derniers et tous les autres, la livraison est en rendu aéroport uniquement) — UE : 90 EUR par envoi — Autres pays d’Europe : 120 EUR par envoi — Hors Europe : 200 EUR par envoi — Coûts d’expédition à la charge de l’acheteur : 55 EUR par envoi e) Hepatitis C virus BRP, B19 virus DNA for NAT: carboglace + marchandises dangereuses – de 5 à 100 flacons (de 1 à 20 unités de vente), expédiés par un transporteur choisi par la DEQM. Pour les commandes supérieures à 100 flacons (20 unités de vente) : prix sur demande (Pour les pays hors France, la livraison est en rendu aéroport uniquement) © European Pharmacopoeia - Catalogue, December 2006 — Autres pays d’Europe : 180 EUR par article (Pour tous les pays de l’UE (à l’exception de Chypre et Malte) la livraison est en rendu domicile. Pour ces derniers et tous les autres, la livraison est en rendu aéroport uniquement) et ces étalons de référence ne peuvent être expédiés en express. — UE : 50 EUR par envoi — Autres pays d’Europe : 125 EUR par envoi — Hors Europe : 125 EUR par envoi h) Matières dangereuses expédiées uniquement par route par un transporteur choisi par la DEQM — UE : 150 EUR par article (rendu domicile) — Autres pays d’Europe : 180 EUR par article (rendu domicile) — Hors Europe : ne peut pas être expédié i) Précurseurs chimiques de stupéfiants (substances contrôlées : expédiées par un transporteur choisi par la DEQM) (Pour les pays hors UE, la livraison est en rendu aéroport uniquement) — France : pas de supplément spécial, le prix s’entend emballage et expédition par la poste compris. Sur demande du client un envoi express est facturé 18 EUR par envoi — UE : 18 EUR par envoi — Autres pays d’Europe : 160 EUR par envoi — Hors Europe : 160 EUR par envoi NB : ces suppléments s’entendent emballage, port et gestion des permis officiels d’exportation j) Psychotropes (substances contrôlées : expédiées par un transporteur choisi par la DEQM) (Pour les pays hors France, la livraison est en rendu aéroport uniquement) — France : pas de supplément spécial, le prix s’entend emballage et expédition par la poste compris. Sur demande du client un envoi express est facturé 18 EUR par envoi — UE (hors France) : 110 EUR par envoi — Hors UE : 160 EUR par envoi ix Catalogue NB : ces suppléments s’entendent emballage, port et gestion des permis officiels d’exportation k) Stupéfiants (substances contrôlées : expédiées par un transporteur choisi par la DEQM) (Pour les pays hors France, la livraison est en rendu aéroport uniquement) — France : 50 EUR par envoi — UE (hors France) : 110 EUR par envoi — Hors UE : 160 EUR par envoi NB : ces suppléments s’entendent emballage, port et gestion des permis officiels d’exportation — adresse de facturation incluant le nom de la société, le code postal, la ville, le pays et le numéro de téléphone — adresse de livraison (si différente) incluant le nom de la société, le code postal, la ville, le pays et le numéro de téléphone (attention ADRESSE COMPLÈTE, pas de boîte postale) — nom du contact, numéro de téléphone, numéro de fax et adresse e-mail: une adresse e-mail est indispensable pour recevoir une confirmation de commande et l’avis d’expédition du paquet — numéro TVA (obligatoire dans l’Union Européenne) — votre numéro/référence de commande l) Spectres de référence — code article — France : pas de supplément spécial, le prix s’entend emballage et expédition par la poste compris. Sur demande du client un envoi express est facturé 18 EUR par envoi — nom officiel de l’étalon de référence tel qu’indiqué dans le catalogue — UE : 18 EUR par envoi — nom et numéro de compte du transporteur si vous désirez utiliser le vôtre — Autres pays : 50 EUR par envoi — nombre d’unités de vente 3. Comment commander Si les bons de commandes ne comportent pas le nom officiel de l’étalon de référence et le code complet (tel qu’indiqué dans le catalogue), la DEQM ne saurait être tenue pour responsable en cas d’envoi d’un mauvais article. Les étalons de référence sont fournis par la DEQM. Malheureusement, il ne nous sera pas possible de traiter les commandes ne contenant pas ces informations. 3.1. BON DE COMMANDE 3.2. QUANTITÉS Veuillez envoyer votre commande en utilisant le bon de commande SCR (voir page xvi du catalogue) ou en envoyant un bon de commande officiel à l’en-tête de votre société à la DEQM. Le bon de commande est également disponible pour téléchargement sur notre site www.pheur.org sous Reference Standards (Ph. Eur. Reference Standards). Un étalon de référence peut être constitué de plusieurs flacons ou ampoules (voir colonne Sale Unit dans le catalogue) ; dans ce cas ne pas commander en nombre de flacons ou ampoules totaux mais en unités de vente. — Coûts d’expédition à la charge de l’acheteur : 10 EUR par envoi. Fax : +33 (0)3 88 41 27 71 à l’attention de la Section Ventes E-mail : [email protected] Courrier : Conseil de l’Europe, Direction Européenne de la Qualité du Médicament, à l’attention de la Section Ventes, 7 allée Kastner, CS 30026, F-67081 Strasbourg, France Les acheteurs sont financièrement responsables des commandes reçues en double dans les cas suivants : — confirmation de commande non clairement indiquée en tant que confirmation d’une commande déjà envoyée au Conseil de l’Europe (DEQM) Exemple : pour recevoir 4 flacons de calcitonine, il faut commander : référence C0200000, quantité 2. La politique de la DEQM est de limiter la quantité d’achat d’un même étalon de référence quand les niveaux de stock sont bas. La DEQM fera tout son possible pour assurer que toutes les commandes soient expédiées en totalité. Cependant, quand les stocks sont limités, la DEQM préparera les commandes de façon que le plus grand nombre d’utilisateurs reçoivent au moins une partie des quantités limitées. 3.3. DOCUMENTATION SPÉCIALE 3.3.1. Pour tout produit Il est de la responsabilité du client de s’assurer que l’importation du produit n’est pas soumise à une autorisation spéciale ou qu’une interdiction d’importation du produit est en vigueur dans son Veuillez noter que nous n’acceptons pas de commandes pays. Tous les documents nécessaires à l’importation doivent être joints à la commande (spécialement pour par téléphone. les produits biologiques). Pour importer en Chine, Si vous n’utilisez pas le bon de commande SCR officiel, un formulaire additionnel doit être complété et doit assurez-vous que les informations suivantes sont fournies accompagner chaque commande d’étalons de référence sur votre bon de commande : (voir modèle inclus dans ce catalogue à la page xix). — envoi d’une même commande à plusieurs reprises (c.-à-d. par fax, e-mail, courrier ou n’importe quelle combinaison citée ci-dessus) x © European Pharmacopoeia - Catalogue, December 2006 Catalogue 3.3.2. Substances contrôlées Veuillez noter : — 3.3.2.1. Psychotropes et stupéfiants de la Convention de Vienne Etant donné que nos locaux se situent sur le territoire français, les mentions « *psy » et « *narc » portées dans le catalogue se réfèrent uniquement à la législation française. — Pour tous les clients de l’UE, excepté la France, toutes les substances psychotropes seront facturées séparément des autres substances et un supplément spécial sera facturé (voir 2.2.h). France : la commande d’une substance psychotrope doit être adressée exclusivement par courrier accompagnée d’une copie de l’autorisation de détention ou d’une copie de la déclaration d’ouverture d’établissement pharmaceutique. Autres pays : la commande d’une substance psychotrope doit être adressée exclusivement par courrier. Ces substances faisant l’objet d’un contrôle à l’importation et à l’exportation dans certains pays, il est de la responsabilité du client de se conformer à la législation du pays importateur et d’obtenir tous les documents nécessaires. Un permis d’importation (en français ou avec une traduction certifiée en français jointe) doit être valide au moins 6 mois à compter de la date de réception du permis par le Conseil de l’Europe (DEQM). — 3.3.2.2. Précurseurs chimiques de stupéfiants (Convention de Vienne) Pays de l’UE : toute commande de substances fréquemment utilisées pour la fabrication illicite de stupéfiants et de substances psychotropes (mention «*Drug precursor» dans le catalogue) doit être accompagnée d’une déclaration d’usage final spécifiant le ou les usages de la (des) substance(s) établie selon le modèle européen en vigueur inclus dans ce catalogue page xviii. Autres pays : il est de la responsabilité du client de se conformer à la législation du pays importateur et d’obtenir tous les documents nécessaires à l’importation. Un permis d’importation (en français ou avec une traduction certifiée en français jointe) doit être valide au moins 6 mois à compter de la date de réception du permis par le Conseil de l’Europe (DEQM). Un supplément spécial est demandé (voir 2.2.h et 2.2.i). Les permis d’export pour les substances psychotropes et pour les précurseurs sont nécessaires avant de pouvoir réaliser l’envoi. 3.4. TRAITEMENT DE LA COMMANDE ET FACTURATION A réception d’une commande complète, la DEQM s’efforce de facturer et d’expédier la commande en 2-3 jours ouvrés à l’exception : — Pour tous les clients hors UE, toutes les substances psychotropes et tous les précurseurs seront facturés séparément des autres substances et dans tous les cas un supplément spécial sera facturé (voir 2.2.h et 2.2.i). — Pour tous les clients de l’UE, toute commande de précurseurs doit être accompagnée de la déclaration d’usage final valide. Un modèle est inclus dans ce catalogue à la page xviii. Des retards dans l’expédition des produits seront inévitables si l’ensemble de la documentation n’est pas fourni lors de la commande. C’est pourquoi nous demandons que toutes les substances contrôlées soient commandées séparément des autres étalons de référence. 4. Règlement Le règlement peut s’effectuer par chèque à l’ordre du Conseil de l’Europe/DEQM et être envoyé à l’adresse cidessus (voir 3.1) ou par transfert bancaire. Société Générale, 255, route de Mittelhausbergen, 67200 Strasbourg, France IBAN Account Number for International Transfers: (FR 76) 30003 02360 00550034256 76 National transfers: 30003 02360 00550034256 76 SWIFT: SOGEFRPP Il est également possible de régler par carte de crédit (Visa, Eurocard, Mastercard ou American Express) en indiquant le numéro de la carte, la date d’expiration, le nom du titulaire de la carte et en n’oubliant pas la signature du titulaire. Veuillez noter que nous ne prenons pas de numéro de carte bancaire par téléphone. Dans tous les cas, le règlement doit être net de frais pour le Conseil de l’Europe et les factures sont payables à 30 jours date de facture. Tout autre frais, tels que droits de douane ou taxes sont à la charge de l’acheteur. Pour certains pays, notamment ceux ayant des réglementations monétaires strictes, pour de nouveaux clients, pour d’importantes commandes, nous nous réservons le droit de demander un paiement par avance. En cas de doute, veuillez nous contacter à [email protected]. Le règlement par lettre de crédit n’est pas accepté. 5. Procédures réglementaires et SH/NDP En cas de disposition particulière dans le pays de l’acheteur, ce dernier devra détenir les autorisations — des commandes de substances contrôlées, d’importation et avoir réglé les éventuelles questions réglementaires avant la commande et l’expédition des — des envois effectués sous glace (ceux-ci ne sont produits. En cas de blocage douanier au moment de réalisés que les lundis et mardis) et carboglace (ceux- l’importation dans le pays de l’acheteur, ce dernier ci ne sont réalisés que les lundis), assumera la responsabilité pleine et entière. Le Conseil de l’Europe (DEQM) ne pourra en aucun cas intervenir dans — des commandes pour lesquelles un prépaiement est une quelconque assistance. requis. © European Pharmacopoeia - Catalogue, December 2006 xi Catalogue Origine des produits : Diplomatique, Conseil de l’Europe la législation du pays où les produits sont livrés. Il appartient au client de vérifier auprès des autorités - France. locales les possibilités d’importation ou d’utilisation des SH/NDP 000009. produits ou services qu’il envisage de commander. Le NDP-SH est strictement limité aux opérations Le client est seul responsable du choix des produits, de d’exportation de la France. leur conservation à compter de la livraison et de leur L’importateur fera son affaire personnelle pour la utilisation. En aucun cas le Conseil de l’Europe (DEQM) classification tarifaire dans son pays et assumera les ne pourrait être tenu responsable de tout dommage obligations réglementaires, fiscales, sanitaires et intervenant de ce fait. sécuritaires qui en découlent. Le Conseil de l’Europe (DEQM) garantit que les produits sont en parfait état lors de la remise au transporteur. Ceci 6. Réclamation est la seule garantie consentie par le Conseil de l’Europe (DEQM). Aucune autre garantie expresse ou tacite n’est Réclamations liées à la livraison accordée. En particulier, le Conseil de l’Europe (DEQM) Les retards éventuels ne donnent pas droit à l’acheteur ne saurait garantir que les produits répondent aux d’annuler la vente, de refuser la marchandise ou de attentes spécifiques du client. réclamer des dommages et intérêts. Le Conseil de l’Europe (DEQM) ne saurait être tenu pour L’acheteur ne peut émettre des réserves lors de la responsable de l’inexécution du contrat conclu en cas de livraison des produits qu’en cas de livraison non rupture de stock ou indisponibilité du produit, de force conforme quantitativement et qualitativement (au cas majeure, de perturbation ou grève totale ou partielle où le paquet contenant les produits serait fortement notamment des services postaux et moyens de transport, endommagé). d’inondation ou d’incendie. Ces réserves doivent être faites par écrit auprès du 8. Litiges transporteur lors de la livraison. Une copie de ces réserves doit être envoyée au Conseil de En conformité avec les dispositions de l’article 21 de l’Europe (DEQM) (par courrier électronique ou télécopie) l’accord général sur les privilèges et immunités du Conseil de l’Europe, tout litige entre le Conseil de au plus tard 12 heures après que ces réserves ont été l’Europe (DEQM) et le client relatif à l’application des faites. présentes conditions générales sera soumis, à défaut de Réclamations liées à la commande règlement amiable entre les deux parties à un arbitrage selon les modalités déterminées par l’Arrêté N° 481 du Le client ne peut faire de réclamation lors de la livraison Secrétaire Général, approuvé par le Comité des Ministres. des produits qu’en cas de non conformité quantitative par rapport à sa commande initiale. Pour tout renseignement concernant : Etalons de référence – Renseignements concernant les Toute éventuelle réclamation devra être transmise dans commandes, la facturation et l’expédition les 48 heures à compter de la réception du produit dans Helpdesk: http://www.pheur.org/hd son emballage d’origine. Fax: +33 (0)3 88 41 27 71 Concernant les envois en rendu aéroport, toute Détails des vols - Questions concernant les expéditions éventuelle réclamation devra être transmise dans (uniquement pour les commandes SCR) la semaine à compter de la date d’arrivée du colis à Helpdesk: http://www.pheur.org/hd l’aéroport. E-mail: [email protected] S’il est prouvé que les réserves ou réclamations faites au Fax: +33 (0)3 88 41 27 71 moment de la livraison sont dues au fait que le paquet et les produits sont fortement endommagés, ou qu’il y a Monographies - Questions concernant les monographies erreur manifeste, le Conseil de l’Europe (DEQM), à son Helpdesk: http://www.pheur.org/hd choix, établira un avoir ou remboursera au client le prix Fax: +33 (0)3 88 41 27 71 payé ou effectuera une nouvelle livraison de produits similaires. La version électronique du catalogue des étalons de référence (nécessite Adobe Acrobat version 5) ainsi que En cas de réclamation, les frais de transport et autres d’autres informations sont disponibles sur notre site frais (douane) pour le retour des produits au Conseil de www.pheur.org l’Europe (DEQM) sont à la charge de l’acheteur. L’acheteur ne peut en aucun cas retourner les produits au Conseil de l’Europe (DEQM) sans en avoir averti celuici et obtenu son accord écrit. II. CONDITIONS DE STOCKAGE LONG TERME À LA DEQM Aucun retour de produits ne sera accepté et nous ne procéderons à aucun échange si les conditions énoncées et la procédure ci-dessus n’ont pas été respectées. Voir colonne spécifique (Storage) dans la liste débutant page 1. 7. Responsabilité III. IDENTIFICATION DES ÉTALONS DE RÉFÉRENCE La responsabilité du Conseil de l’Europe (DEQM) ne saurait être engagée en cas de non-respect de La dénomination des étalons de référence reprise dans ce catalogue correspond au nom anglais utilisé dans les xii © European Pharmacopoeia - Catalogue, December 2006 Catalogue monographies officielles de la Ph. Eur. et classé par ordre alphabétique (nom en italique suivi de SCR ou PBR). IV. UTILISATION DES ÉTALONS DE RÉFÉRENCE Les étalons de référence de la Ph. Eur. sont établis et distribués selon le principe général de la norme ISO 34. La spécificité des étalons de référence des pharmacopées a été officiellement reconnue dans l’introduction de la révision de la norme ISO 34 - Exigences générales pour la compétence des producteurs de matériaux de référence - deuxième édition 2000) : « Les étalons et les substances de référence des pharmacopées sont établis et distribués par les autorités de pharmacopée selon le principe général de ce guide. Il convient toutefois de noter que chaque autorité de pharmacopée adopte une approche différente pour transmettre aux utilisateurs les informations fournies par le certificat d’analyse et les dates d’expiration. L’incertitude sur les valeurs assignées aux étalons et substances de référence est négligeable par rapport aux limites définies dans les dosages (méthodes spécifiques) des pharmacopées pour lesquelles elles sont utilisées. En conséquence, cette incertitude n’est pas mentionnée. » Les étalons de référence sont des lots spécialement sélectionnés et vérifiés, appropriés à l’usage prescrit dans la Pharmacopée. La colonne « Monograph » liste la(les) monographie(s) et/ou la(les) méthode(s) analytique(s) générale(s) dans lesquelles sont utilisés les étalons de référence. Les numéros de monographie comportent quatre digits (par exemple la monographie 0076), les chapitres généraux comportent cinq digits (par exemple le texte 5.4 est indiqué par le nombre 50400, la méthode 2.5.1 est indiquée par le nombre 20501). Ces nombres sont disponibles au début de la monographie et correspondent au numéro d’identification du document. L’utilisation de ces produits pour d’autres usages que ceux prescrits dans la monographie de la Ph. Eur. relève de la responsabilité de l’utilisateur. Chaque flacon ou ampoule fourni contient une quantité de produit suffisante pour l’utilisation prescrite. Un flacon ou une ampoule est considéré comme un étalon de référence à « utilisation immédiate ». Nous recommandons que le contenu d’un flacon ou d’une ampoule soit utilisé dans la même série d’analyses. Il convient de ne commander que la quantité nécessaire pour le besoin immédiat et d’utiliser les étalons de référence dans les meilleurs délais possibles. La stabilité du contenu des flacons ouverts ne peut être garantie. Dans des cas spécifiques, un lot peut faire l’objet d’une présentation en sous-lots 1.1, 1.2, 1.3, etc. pour des raisons de remplissage ou d’étiquetage. (Note : l’ancienne numérotation des sous-lots 1a, 1b, 1c sera progressivement remplacée par 1.1, 1.2, 1.3, etc.) qui adopte les rapports d’études les ayant qualifiés pour leur usage, il n’est fourni avec les étalons de référence ni certificat d’analyse, ni données autres que celles requises pour l’utilisation prévue par la monographie de la Ph. Eur. De la même façon, il n’est pas indiqué de date de péremption car les étalons de référence sont conformes aux exigences de la monographie correspondante et font l’objet de vérifications régulières. Dans la colonne Information du catalogue est rendue officielle la date de fin de validité comme SCR/PBR des lots qui viennent d’être remplacés. Ainsi «batch 1 valid until 30 June 2006» signifie que le lot 1 n’est plus officiel à partir du 1er juillet 2006. Lorsqu’il n’est pas fait mention de conditions de dessiccation, les substances et préparations sont à utiliser en l’état. Pour les SCR avec une valeur assignée, la valeur est exprimée sur la substance « telle quelle ». La disponibilité des étalons dans la base de données des étalons de référence sur notre site internet est mise à jour quotidiennement. Des informations sur l’origine, la valeur assignée et la validité du lot sont également disponibles. Une déclaration de validité de lot (BVS) pour les étalons de référence est maintenant disponible. L’utilisateur d’étalons de référence peut imprimer cette déclaration de validité à partir de la base de données Reference Standards du site internet de la DEQM (http://crs. pheur.org/). Cet outil aidera les utilisateurs à assurer la traçabilité des dates de validité et des notices distribuées avec le lot précédent. Un exemple de BVS est inclus dans ce catalogue pages xx et xxi. Pour les étalons de référence conditionnés en ampoules de verre scellées, la procédure à suivre pour l’ouverture est la suivante : tapoter doucement l’ampoule pour rassembler son contenu dans le fond ; faire une entaille sur l’ampoule avec une lime ; chauffer à blanc une tige de verre et l’appuyer fermement sur l’entaille ; s’il ne se produit pas de cassure, approfondir et agrandir l’entaille, chauffer à nouveau la tige et recommencer. Substances toxiques. Certains étalons de référence sont très toxiques et doivent être manipulés avec des précautions particulières afin d’éviter tout contact. Il est recommandé de manipuler ces substances dans une boîte à gants ou, à défaut, en portant des gants, une protection oculaire et un masque. Préparations biologiques et produits du sang. Ces préparations sont à considérer comme potentiellement dangereuses pour la santé et doivent être utilisées et détruites conformément aux pratiques de sécurité de votre propre laboratoire. Fiches de données de sécurité Les fiches de données de sécurité sont disponibles sur notre site internet ou sur demande. Les renseignements présentés dans les fiches de données de sécurité et fournis par la Ph. Eur. proviennent Toutefois, toutes les précautions sont prises pour garantir des informations transmises habituellement par le l’homogénéité de qualité et des spécifications des sousfournisseur ou fabricant du produit. Elles n’ont pas été lots entre eux. vérifiées indépendamment par les agents de la Ph. Eur. Les SCR et PBR étant des produits faisant l’objet d’une L’exactitude de ces renseignements ne peut donc être certification officielle par la Commission de la Ph. Eur. garantie. © European Pharmacopoeia - Catalogue, December 2006 xiii Catalogue V. NOTICE Dans certains cas, une notice explicative est envoyée avec le produit. Voir colonne spécifique (Leaflet) dans la liste débutant page 1 (si aucune indication n’est mentionnée, il n’y a pas de notice pour le produit concerné). Les notices sont également disponibles sur notre site internet. xiv © European Pharmacopoeia - Catalogue, December 2006 Council of Europe European Directorate for the Quality of Medicines CRS Order Form Tel: +33 (0)3 88 41 30 30 7 allée Kastner, CS 30026, F-67081 Strasbourg (France) website: http://www.pheur.org Helpdesk: http://www.pheur.org/site/page_521.php SIRET: 778860080010 APE Code APE:990Z VAT N°: Not applicable to Council of Europe - diplomatic privilege. Fax: + 33 (0)3 88 41 27 71 BILLING ADDRESS Your Client Code Company Name* Invoice Address* DELIVERY ADDRESS City* PostCode* Country* City* PostCode* Country* Contact Name* VAT N°(* in Europe) Tel* E-mail Contact Name* VAT N°(* in Europe) Tel* Email (Please complete if different from invoicing address) Company Name* Delivery Address* Fax Fax All items marked with an asterisk (*) are mandatory Your Order Reference* [reference] Reference* Date* Item* Unit Price (1) A CRS/BRP may include several individual vials (see sale unit in catalogue), in such instances do not order in terms of total number of vials. Total Goods/€ DELIVERY CHARGES and PRICES The price should not be regarded as representing the selling price of a commercial product. The prices quoted in our catalogue are exclusive of duties and taxes. Extra handling charges may be applied. Please see our catalogue for details. CONDITIONS OF SALE We sell on our standard terms of business. For details please see our catalogue. Payment I would like to pay now. I will automatically receive an invoice/receipt I enclose a cheque made payable to Council of Europe/EDQM I wish to pay by credit card Visa N° Expiry Date I will pay on receipt on a invoice Euro/Mastercard N° Name American Express N° Signature Quantity(1)* Total Conseil de l’Europe Direction Européenne de la Qualité du Médicament Bon de Commande SCR Tél: +33 (0)3 88 41 30 30 7 allée Kastner, CS 30026, F-67081 Strasbourg (France) site internet : http://www.pheur.org Helpdesk : http://www.pheur.org/site/page_521.php SIRET : 778860080010 APE Code APE:990Z N° TVA : non applicable au Conseil de l’Europe - régime diplomatique Fax : + 33 (0)3 88 41 27 71 ADRESSE DE FACTURATION Votre Code Client Nom de la société* Adresse de facturation* ADRESSE DE LIVRAISON Ville* Code postal* Pays* Ville* Code postal* Pays* Nom du Contact* TVA N°(* en Europe) Tél* E-mail Nom du Contact* TVA N°(* en Europe) Tél* E-mail (Veuillez compléter si différent de l’adresse de facturation) Nom de la Société* Adresse de livraison* Fax Fax Les informations marquées du symbole*sont obligatoires. Votre N° de Commande* [référence] Référence* Date* Item* Prix unitaire Total Produits € (1) Une SCR/PBR peut être constituée de plusieurs flacons, dans ce cas ne pas commander en nombre de flacons totaux. FRAIS DE LIVRAISON et PRIX Le prix n’est pas à considérer comme le prix de vente d’un produit commercial. Les prix indiqués dans notre catalogue s’entendent hors droits et taxes. Des frais de livraison peuvent s’appliquer. Voir notre catalogue pour plus de détails. CONDITIONS DE VENTE Les conditions générales de vente sont celles figurant dans notre catalogue. Paiement Je désire payer maintenant, je recevrai automatiquement une facture acquittée Je joins un chèque à l’ordre du Conseil de l’Europe/DEQM Visa N° Je désire payer par carte de crédit Euro/Mastercard N° Expire à fin : Je réglerai à réception de facture Nom Quantité(1)* American Express N° Signature Total COMPANY LETTERHEAD CUSTOMER DECLARATION OF SPECIFIC USE(S) OF THE SCHEDULED CATEGORY 1 OR 2 SUBSTANCE (INDIVIDUAL TRANSACTIONS) I, We, Name …………………………………………………………………………………………… Address …………………………………………………………………………………………. Authorisation/Licence/Registration No. or reference1 ………………………………………….. Issued on …………..…………….…. by ……………………………………………………… (name and address of authority) and valid until/without expiry1………………………………...................................................... have ordered from: Name …………………………………………………………………………………………… Address …………………………………………………………………………………………. the following substances (name and CN code2) …………………………………………… .. (quantity) ……………………… ..................................................... The substance will be used solely for ………………………………………………………….. We confirm that the substance referred to above will only be re-sold or otherwise supplied to a customer on the condition that the customer will furnish a similar declaration of use or, for category 2 substances, a declaration relating to multiple transactions. Signed ……………………………………. Name …………………………………… (block capitals) Position …………………………………... Date ……………………………………. 1 2 Delete as appropriate Combined Nomenclature code EN-TÊTE DE LA SOCIÉTÉ DÉCLARATION DU CLIENT SPÉCIFIANT L’USAGE OU LES USAGES DE LA SUBSTANCE RELEVANT DES CATÉGORIES 1 OU 2 (TRANSACTIONS INDIVIDUELLES) Nous, Nom…………………………………………………………………………………………………… Adresse ……………………………………………………………………………………………………….... Référence à l’autorisation/l’agrément/l’enregistrement1 ……………………………………………... Délivré le …………..…………….…. par …………………………………………………………… (nom et adresse de l’autorité) et valable jusqu’au/sans limite de temps1………………………………….. ........................................ avons commandé à : Nom…………………………………………………………………………………………………… Adresse …………………………………………………………………………………………….…. La substance suivante (dénomination et code NC2) .. …………………………………………….... (quantité)........................................................................................................ La substance sera utilisée exclusivement pour ………………………...………………………….. Nous certifions que la substance visée ci-dessus ne sera revendue ou transférée à un client qu’à la condition que ce client fournisse une déclaration d’utilisation conforme à ce modèle ou, pour les substances de catégorie 2, une déclaration relative à des transactions multiples. Signature……………………………………….. Nom …………..……………………………… (en majuscules) Quantité …………………………………... Date ……………………………………. 1 2 Biffer la mention inutile Code de la nomenclature combinée COMPANY LETTERHEAD IMPORT OF EUROPEAN PHARMACOPOEIA REFERENCE STANDARDS INTO CHINA I, We, Name ………………………………………………………………………………….………………. Address ………………………………………………………………………………………………………… ………………………………………………………………………………………………………… Hereby confirm that: - The substances below are not controlled in China1 We have all the import authorisations/licences for the import of the substances below into China1 We have the authorisations/licences to pay in Euro currency1 List of substances Name CRS Code Quantity The Council of Europe (EDQM) cannot be held responsible for failure to meet the requirements of the legislation of China. It is the customer’s responsibility to check with the local authorities to make sure that the goods they intend to order can be imported into or used in China. I, We, agree If the parcel is held up by the Chinese customs or is unable to clear customs - To pay the invoice in full - To bear any shipping or other costs (customs) incurred to return goods to the Council of Europe (EDQM). Signed ……………………………………. Name …………………………………… (block capitals) Position …………………………………... Date ……………………………………. 1 Delete as appropriate http://crs.pheur.org/db/4DCGI/www_BVS BATCH VALIDITY STATEMENT EUROPEAN PHARMACOPOEIA REFERENCE STANDARDS (CRS) & (BRP) This Batch Validity Statement has to be used in conjunction with Ph. Eur. general chapter 01/2007:51200 Reference Standards. European Directorate for the Quality of Medicines (EDQM) – Council of Europe Postal address: B.P. 907 - F 67029 Strasbourg Cedex 1 Phone: +33 (0)3 88 41 30 30 Fax: +33 (0)3 88 41 27 71 Internet : http://www.pheur.org Name Insulin (human) Catalogue code I0310000 Batch number* 3 Assigned value 7.03 mg insulin + A21 desamido per vial Validity Batch 3 is valid at the printing date: 2006-8-22 Storage conditions The standard is intended for immediate use. Recommended EDQM storage conditions for unopened containers : -20°C Safety data Safety Data Sheet is available from the detailled view or upon request. Leaflet Click on the hyperlink to download the leaflet containing the instructions for use, if available (Adobe Acrobat Reader version 5 or higher, or the corresponding browser plug-in is needed to open the file) click to download the leaflet * Sub-batches a, b, c are obtained from the same batch of bulk material and the quality does not differ from one sub-batch to another. This statement is valid at the date of printing : 2006-8-22 Legal notice: The Council of Europe (EDQM) makes no representation or warranty with respect to the accuracy, completeness, or currentness, of this electronic statement. The Council of Europe (EDQM) shall not be liable on account of any potential errors or omissions. 1 sur 1 22/08/06 14:14 n/a 1 1 1 2 2 1 1 2 5 4 1 1 3 1 1 1 2 5 2 2 2 1 1 3 2 Y0000056 Aceclofenac - reference spectrum Y0000085 Aceclofenac impurity F Y0000086 Aceclofenac impurity H Acenocoumarol Acesulfame potassium Acesulfame potassium impurity B Acetazolamide Acetylcholine chloride Acetylcysteine Acetylcysteine impurity C Acetylcysteine impurity D ß-Acetyldigoxin ß-Acetyldigoxin for peak identification Acetylsalicylic acid N-Acetyltryptophan N-Acetyltyrosine Acholeplasma laidlawii BRP Aciclovir Aciclovir impurity A A0050000 A0070000 A0070020 A0100000 Y0000002 A0150000 A0152000 A0153000 Y0000565 Y0000642 A0200000 A0208000 A0202000 Y0000693 A0220000 A0221000 A0225000 Acitretin Y0000360 Acriflavinium monochloride A0230000 Adenine A0230200 Adenosine Y0000110 Adipic acid A0300000 Adrenaline tartrate A0325000 Alanine © Council of Europe, all rights reserved 2006 n/a 1 1 1 1 1 1 Batch 1 2 Acamprosate calcium - reference spectrum Acamprosate impurity A Acarbose Acarbose for identification Acarbose for peak identification Acebutolol hydrochloride Acebutolol impurity B Reference Standard Y0000127 Acebutolol impurity C Y0000128 Acebutolol impurity I Order Code Y0000055 Y0000116 Y0000500 Y0000354 Y0000427 A0040000 Y0000359 Catalogue No. 48-2006/4 100 mg 1 mg 50 mg 50 mg 50 mg 200 mg 50 mg 20 mg 50 mg 10 mg 100 mg 50 mg 50 mg 10 mg 10 mg 30 mg 10 mg 100 mg 125 mg 200 mg 1 ml 75 mg 15 mg n/a 20 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0871 0871 1585 1585 2089 2089 2089 0871 0871 Monograph 1 Batch 1 is valid until 28 February 2007 2-[(2-amino-6-oxo-1,6-dihydro-9§-purin-9-yl)methoxy]ethyl acetate 99.7% CœŒHœÿO– ; Batch 1 is valid until 28 February 2007 90.9% CŒÕHŒÿNœOÿSœ; N,N'-diacetyl-L-cystine N,£-diacetyl-L-cysteine Batch 1 is valid until 30 April 2006 5-chloro-6-methyl-1,2,3-oxathiazin-4(3§)-one 2,2-dioxide Yes Yes Yes +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -80°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a c a a a f f a a a d a a l a a a a 79 79 79 79 79 79 79 79 79 120 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 l 79 a 79 a 79 a 79 a 79 a 79 a 1385 +5°C g 2043 Yes +5°C a 0800,1486 +5°C a 1486 +5°C a 1586 +5°C a 0254,0285,0732 +5°C g 0614,0752 +5°C a For extra charges please see 2.2 0698,0699 1282 1282 0454 1485,1971 0967 0967 0967 2168 2168 0309 1383 1384 20607 0968 0968 1281 benzyl[[[2-[(2,6-dichlorophenyl)amino]phenyl]acetyl]oxy]acetate 1281 [[[[[[[2-[(2,6-dichlorophenyl)amino]phenyl]acetyl]oxy]acetyl] 1281 oxy]acetyl]oxy]acetic acid Information Unit Sale Quantity Unit n/a 1 50 mg 1 3-aminopropane-1-sulphonic acid 100.1 mg 1 100.1 mg per vial of Cœ—H÷–NOŒ‡ 10 mg 1 40 mg 1 50 mg 1 10 mg 1 N-[3-acetyl-4-[(2RS)-2-hydroxy-3-[(1-methylethyl)amino] propoxy]phenyl]acetamide (diacetolol) 20 mg 1 N-(3-acetyl-4-hydroxyphenyl)butanamide 0.004 mg 1 N-[3-acetyl-4-[(2RS)-3-(ethylamino)-2-hydroxypropoxy]phenyl] butanamide 6 December 2006 Allopurinol impurity D Allopurinol impurity E Allylstrychnine bromide Almagate Almagate - reference spectrum Alprazolam - * psy Alprenolol hydrochloride Alprostadil Altizide Alverine citrate Alverine for peak identification Alverine impurity D Amantadine hydrochloride Ambroxol hydrochloride Amfetamine sulphate - reference spectrum Amidotrizoic acid dihydrate Amikacin Amikacin impurity A © Council of Europe, all rights reserved 2006 A0365900 Amikacin sulphate A0370000 Amiloride hydrochloride A0350040 A0350050 A0351000 Y0000235 Y0000255 A0357000 A0360000 Y0000054 Y0000606 New Y0000687 New Y0000595 New Y0000607 A0363000 A0363700 A0900000 A0365000 A0368000 A0368010 2 1 2 1 1 1 n/a 1 1 1 1 1 1 1 1 2 n/a 1 1 1 2 2 A0350020 Allopurinol impurity B A0350030 Allopurinol impurity C 1 1 4 n/a 2 n/a 1 1 Batch 1 2 2 Albendazole Alcuronium chloride Alfacalcidol Alfacalcidol - reference spectrum Alfadex Alfentanil hydrochloride - reference spectrum Alfuzosin hydrochloride Alfuzosin impurity A Reference Standard A0349000 Allantoin A0350000 Allopurinol New A0350010 Allopurinol impurity A Order Code A0325100 A0325200 A0325450 A0325451 A1225000 A0325500 A0325800 A0325801 Catalogue No. 48-2006/4 200 mg 100 mg 10 mg 20 mg 10 mg 25 mg n/a 125 mg 100 mg 50 mg 5 mg 5 mg 0.125 mg 10 mg 100 mg 125 mg n/a 100 mg 200 mg 10 mg 10 mg 10 mg 60 mg 50 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 2 Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C Leaflet Storage a a a a a a l j a a a a a a a a l a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 300 c 79 l 79 a 79 l 79 a 79 a For extra charges please see 2.2 0576 0576 1285 2010 2010 1065 0628,0876 1488 0370 2156 2156 2156 0463 1489 0368 0873 1289 1289,1290 0576 0576 1288 0576 0576 1386 1285 1286 1286 1070,1487 1062 1287 1287 Monograph 93.1% CœœH÷–N—OŒ– 86% CœœH÷–N—OŒ–; 4-O-(3-amino-3-desoxy-alpha-D-glucopyranosyl)-6-O-(6-amino-6 -desoxy-alpha-D-glucopyranosyl)-N1-[(2S)-4-amino-2hydroxybutanoyl]-2-desoxy-L-streptamine 89.0% CœœH÷ŸN—OœŒSœ 1290 0651 N-(3-cyclohexylpropyl)-N-ethyl-3-phenylpropan-1-amine 99.2% CœÕH–÷O— 13.4% carbonic acid 99.9% C—H÷N÷O 5-amino-1H-pyrazole-4-carboxamide ; Batch 1 is valid until 28 February 2007 5-formylamino-1H-pyrazole-4-carboxamide N-(4H-1,2,4-triazol-4-yl)-1H-pyrazole-4-carboxamide ; Batch 1 is valid until 31 May 2006 ethyl 5-amino-1H-pyrazole-4-carboxylate ethyl 5-(formylamino)-1H-pyrazole-4-carboxylate Information Unit Sale Quantity Unit 50 mg 1 100 mg 1 5 mg 1 99.9% CœŸH÷÷Oœ ; Batch 3 is valid until 30 April 2006 n/a 1 150 mg 1 89.5% [CÿHŒÕ0—] n/a 1 50 mg 1 20 mg 1 N-[3-[(4-amino-6,7-dimethoxyquinazolin-2-yl) (methyl)-amino]propyl]furan-2-carboxamide 6 December 2006 1 1 1 1 Y0000130 A0590000 A0590002 A0590004 500 mg 500 mg 100 mg 1 1 3 2 3 2 3 1 n/a 4 4 Y0000005 Amphotericin B A1000000 Ampicillin (anhydrous) A1100000 Ampicillin trihydrate A1200000 A1210000 Y0000172 A1220000 A1230000 © Council of Europe, all rights reserved 2006 Anhydrotetracycline hydrochloride Antazoline hydrochloride Apomorphine hydrochloride - reference spectrum Alpha-apo-oxytetracycline Beta-apo-oxytetracycline n/a n/a 10 mg 50 mg n/a 20 mg 20 mg 150 mg 500 mg 250 mg n/a 150 mg n/a n/a 3 n/a 20 mg 50 mg 40 mg 10 mg 20 mg 100 mg 20 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 3 94.2% CœœHœœNœOŸ 960 IU per mg 98.0% CŒÿHŒ„N–O÷S 85.4% CŒÿHŒ„N–O—S 99.9% CœÿH–ŒClNœO‡S [(2RS)-1-ethylpyrrolidin-2-yl]methanamine 4-amino-N-[[(2RS)-1-ethylpyrrolidin-2-yl]methyl]-5-(ethyl sulphonyl)-2-hydroxybenzamine Batch 2 is valid until 28 February 2007 (2-butyl-benzofuran-3-yl)-(4-hydroxy-3,5-diiodophenyl) methanone (2-butyl-benzofuran-3-yl)-(4-hydroxyphenyl)methanone Information Unit Sale Quantity Unit 10 mg 1 methyl-3,5-diamino-6-chloropyrazine-2-carboxylate 60 mg 1 50 mg 1 100 mg 1 125 mg 1 20 mg 1 (3¢£)-3-(3-aminophenyl)-3-ethylpiperidine-2,6-dione; (3-aminoglutethimide) 10 mg 1 3,3'-[diazenediyldi(4,1-phenylene)]bis(3-ethylpiperidine-2,6dione); (azoglutethimide) A0600000 Amitriptyline hydrochloride - reference spectrum Y0000049 Amlodipine besilate Y0000302 Ammonio methacrylate copolymer(type A) - reference spectrum Y0000303 Ammonio methacrylate copolymer(type B) - reference spectrum A0650000 Amobarbital - * psy A0700000 Amobarbital sodium - * psy A0800000 Amoxicillin trihydrate Amiodarone impurity E Amisulpride Amisulpride impurity A Amisulpride impurity B 1 3 1 A0560000 5-Amino-2,4,6-tri-iodo-N-methylisophthalamic acid A0575000 Amiodarone hydrochloride Y0000129 Amiodarone impurity D 2 1 1 1 1 1 Batch 1 Amiloride impurity A 4-Aminobenzoic acid Aminocaproic acid 7-Aminodesacetoxycephalosporanic acid Aminoglutethimide Aminoglutethimide impurity A Reference Standard A0496020 Aminoglutethimide impurity D Order Code Y0000020 Y0000173 A0420000 A0460000 A0496000 A0496005 Catalogue No. 48-2006/4 Yes +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a l a a a c a j j a l l a l a a a a a g a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a For extra charges please see 2.2 0594 0166 0167,0168,0260, 0577,0578,0813, 1140,1653 1292,20702 0167,0168,0578, 1168,1169 0168,0260,0577, 0578,0808,2211, 2212 0210,0211,1654 0972 0136 0198 0198 2082 0464 1491 2081 0803 1490 1490 1490 0751 0803 0803 1291 0651 1687 0874 0708,0813 1291 1291 Monograph 6 December 2006 1 2 2 1 Y0000304 A1271000 Y0000079 Y0000080 Aspartic acid Astemizole Atenolol Atenolol for column validation Atracurium besilate Atracurium for impurity F identification Atracurium for peak identification Atropine sulphate Atropine - reference spectrum Atropine for system suitability Azaperone Azathioprine Azelastine hydrochloride Azelastine impurity B Azelastine impurity D Azelastine impurity E Azithromycin Azithromycin for peak identification Azithromycin for system suitability Azithromycin impurity A Azithromycin impurity B A1330000 A1335000 A1340000 A1341000 Y0000424 Y0000503 Y0000504 A1400000 Y0000231 Y0000230 Y0000029 A1500000 Y0000326 Y0000327 Y0000328 Y0000329 Y0000306 Y0000637 Y0000641 Y0000307 Y0000308 © Council of Europe, all rights reserved 2006 2 n/a 1 2 3 Ascorbic acid Ascorbyl palmitate - reference spectrum Asparagine monohydrate Aspartame Aspartame impurity A A1300000 A1315000 Y0000305 A1320000 A1321000 2 1 2 5 1 1 1 3 n/a 1 1 1 1 1 1 1 1 1 1 1 2 1 Y0000081 Articaine impurity E Arginine aspartate Arginine hydrochloride Articaine hydrochloride Articaine impurity A 2 1 2 Batch Order Reference Standard Code A1250000 Aprotinin solution BRP A1269000 L-Arabinitol A1270000 Arginine Catalogue No. 48-2006/4 50 mg 150 mg 100 mg 100 mg 120 mg 5 mg 5 mg 50 mg n/a 0.4 mg 50 mg 100 mg 25 mg 5 mg 5 mg 5 mg 120 mg 15 mg 0.05 mg 10 mg 0.04 mg 100 mg n/a 60 mg 40 mg 10 mg 10 mg 20 mg 50 mg 100 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 4 6-demethylazithromycin 3-deoxyazithromycin 1-benzoyl-2-[(4RS)-1-methylhexahydro-1H-azepin-4-yl]diazane 4-(4-chlorobenzyl)phthalazin-1(2H)-one 3-(4-chlorobenzilidene)isobenzofuran-1(3H)-one 93.2% C–‡HŸœNœOŒœ 98.9% Cÿ—H‡œNœOŒ‡Sœ 2-(5-benzyl-3,6-dioxopiperazin-2-yl) acetic acid (diketopiperazine) ; Batch 2 is valid until 31 December 2005 Batch 1 is valid until 30 September 2006 methyl3-[[2-(propylamino)acetyl]amino]-4-methylthiophene-2carboxylate methyl 4-methyl-3-[[( 2RS)-2-[(1-methylethyl)amino] propanoyl]amino] thiophene-2-carboxylate Vitamin C Batch 1 is valid until 31 October 2006 Information Unit Sale Quantity Unit 0.5 ml 1 About 27 Ph. Eur. Units per ml 10 mg 1 50 mg 1 Batch 1 is valid until 31 October 2006 Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a f f f a l a a a a a a a a a a a a a l a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a For extra charges please see 2.2 0750,0797 1067 0703 0703 1970 1970 1970 0068,2056 2056 2056 1708 0369 1633 1633 1633 1633 1649 1649 1649 1649 1649 0253,0958 0807 2086 0973 0973 1688 0579,0580 1381 0806,0930,1654, 2114 2096 0805,0885,0998 1688 1688 Monograph 6 December 2006 Benserazide hydrochloride Benserazide impurity A Benzarone Benzathine benzylpenicillin B0477000 B0477010 B0490000 B0500000 © Council of Europe, all rights reserved 2006 B0950000 Betadex Y0000391 Betahistine dihydrochloride B0990000 Betahistine mesilate Benzbromarone - reference spectrum Benzethonium chloride Benzocaine Benzophenone Benzyl alcohol Benzyl benzoate - reference spectrum S-Benzylmercaptoacetyltriglycin Benzylpenicillin potassium Benzylpenicillin sodium Beclometasone dipropionate monohydrate Beclometasone dipropionate for system suitability Beclometasone dipropionate for peak identification Bendroflumethiazide Bendroflumethiazide impurity A Benfluorex hydrochloride Benfluorex hydrochloride for system suitability Benperidol Y0000351 Y0000352 Y0000469 B0400000 Y0000564 Y0000044 Y0000043 B0470000 B0505000 B0550000 B0600000 New Y0000647 Y0000167 B0670000 B0680000 B0700000 B0900000 3 2 1 1 1 1 n/a 3 Bacampicillin hydrochloride Bacitracin zinc Baclofen Baclofen impurity A Bambuterol hydrochloride Barbital - * psy Basic butylated methacrylate copolymer -reference spectrum Beclometasone dipropionate anhydrous B0070000 B0100000 B0200000 B0200050 B0250000 B0300000 Y0000295 B0305000 4 1 1 n/a 1 1 1 1 n/a 1 1 7 1 1 1 2 1 1 1 1 1 1 1 1 1 Batch Order Reference Standard Code Y0000285 B19 virus DNA for NAT testing BRP Catalogue No. 48-2006/4 200 mg 50 mg 100 mg n/a 100 mg 50 mg 40 mg 50 mg n/a 10 mg 50 mg 200 mg 1 1 1 1 1 1 1 1 1 1 1 1 5 88.4% [CÿHŒÕO—]Ÿ ; Batch 3 is valid until 31 March 2006 99.4% CŒÿHŒŸNœNaO÷S; Penicillin G sodium Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C -20°C Leaflet Storage a a a l a a a a l a a a a a a a a a a a a a a a a a a a a j l a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 242 e For extra charges please see 2.2 1393 0974 0011,1088 1784 0256 0705 1372 0113,0148,0149 0113,0114,0148, 0149 1070,1487,1804 1665 1071 Information Unit Sale Monograph Quantity Unit 150 mg 5 B19 virus DNA content logŒÕ 5.8 IU per ml for plasma pool testing See leaflet,0557, by NAT 1527,1646 92.9% CœŒHœ‡ClN–OŸS 120 mg 1 0808,0852 150 mg 1 62.9 IU per mg 0465,0466,20702 50 mg 1 0653 50 mg 1 (¢£)-4-amino-3-(4-chlorophenyl)butyric acid lactam 0653 100 mg 1 1293 500 mg 1 0170 n/a 1 1975 150 mg 1 99.1% Cœ‡H–ŸClOŸ 0654,0809,1449, 1709 10 mg 1 1709 10 mg 1 0654,1709 10 mg 1 0654,1709 100 mg 1 0370 5 mg 1 0370 50 mg 1 1601 360 mg 1 1601 100 mg 1 1010,1172,1254, 1708 50 mg 1 1173 20 mg 1 (¢£)-2-amino-3-hydroxypropanohydrazide 1173 10 mg 1 1393 125 mg 1 90.7% C÷‡H—ÿNÿO‡Sœ 0373 24.1% CŒÿHœÕNœ (N,N' - dibenzylethylenediamine) 6 December 2006 1,3-bis(2-acetyl-3-hydroxyphenoxy)-2-propanol Bisacodyl Bisacodyl for peak identification Bisacodyl for system suitability Bleomycin sulphate Bromazepam - * psy Bromazepam for system suitability - * psy Bromhexine hydrochloride Bromhexine impurity C Bromocriptine mesilate Bromocriptine mesilate for system suitability Bromperidol Bromperidol decanoate Brompheniramine maleate Brotizolam - * psy Brotizolam impurity B © Council of Europe, all rights reserved 2006 B1155000 Brucella melitensis Rev. 1 strain BRP - * Biotox B1157300 Budesonide B1143000 New Y0000645 B1145000 Y0000200 B1150000 New Y0000677 B1152000 B1152050 B1153000 Y0000468 Y0000470 Y0000434 Boldine B1142000 Bordetella pertussis mouse antiserum BRP B1130000 New B1140000 Y0000608 Y0000694 B1141000 1 3 3 1 2 2 2 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 3 2 2 1 2 1 1 2 1 1 1 Betamethasone acetate Betamethasone dipropionate Betamethasone sodium phosphate Betamethasone-17-valerate Betamethasone-21-valerate Betaxolol hydrochloride Betaxolol impurity A Bezafibrate Bifonazole Bifonazole impurity B Biotin Biperiden hydrochloride Biperiden impurity A B1030000 B1040000 B1045000 B1054000 B1055000 B1103000 B1103100 B1115000 B1110000 B1110004 B1116000 B1120000 B1121000 Batch 4 Reference Standard Order Code B1000000 Betamethasone Catalogue No. 48-2006/4 1 mg 110 mg 60 mg 10 mg 100 mg 10 mg 30 mg 5 mg 100 mg 60 mg 100 mg 10 mg 10 mg 30 mg 0.5 mg 50 mg 50 mg 10 mg 5 mg 7 mg 100 mg 100 mg 100 mg 100 mg 15 mg 60 mg 10 mg 100 mg 100 mg 10 mg 50 mg 60 mg 30 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Monograph 1396 See leaflet,20716 0562 0595 0595 0595 0976,20702 6 99.8% Cœ—H–÷Oÿ 0793 1075 Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage f a j j a a g g a a a j a a c a a a a a a a a a a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 90 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0778,0879 0879 0706 N-(2-aminobenzyl)-N-methylcyclohexanamine 0706 0596 0596 0616,1178 1397,1431 0977,1196 2197 2-bromo-4-(2-chlorophenyl)-6H-thieno[3,2-f][1,2,4]triazolo[4,3- 2197 a][1,4]diazepine (demethylbrotizolam) 8910 IU per vial; bleomycin Aœ : 67.0%; Bleomycin Bœ : 29.2%; demethylbleomycin Aœ : 2.6% 99.4% CŒ„HœŒNO÷ Anti-PT: 19.5 ELU/vial Anti-FHA: 69 ELU/vial Anti-69k: 17 ELU/vial Anti-Fim 2/3: 28 ELU/vial Batch 1 is valid until 31 December 2006 0312,0354,0388, 0561 0548,0975 0809 Batch 2 is valid until 30 April 2006 0549,0810 0322,0811 0811 1072 (¢£)-3-(4-ethylphenoxy)-1-[(1-methylethyl)amido]propan-2-ol 1072 1394 1395 Bifonazole impurity B trifluoroacetate 1395 Vitamin H 1073 1074 (1RS)-1-[(1SR,2SR,4SR)-bicyclo[2.2.1]hept-5-en-2-yl]-1-phenyl- 1074 3-(piperidin-1-yl)propan-1-ol (endo form) Information Unit Sale Quantity Unit 75 mg 1 Batch 3 is valid until 31 May 2006 6 December 2006 © Council of Europe, all rights reserved 2006 n/a n/a 3 C0226000 Calcitriol - reference spectrum C0249000 Calcium ascorbate - reference spectrum C0250000 Calcium folinate 1 3 1 n/a n/a 1 n/a 7 1 3 6 Cabergoline Caffeine Calcifediol Calcifediol - reference spectrum Calcipotriol (anhydrous) - reference spectrum Calcipotriol monohydrate Calcipotriol monohydrate - reference spectrum Calcitonin (salmon) Y0000472 C0100000 C0166000 C0166001 Y0000499 Y0000473 Y0000474 C0200000 n/a n/a 1 n/a 1 1 1 1 1 3 1 1 1 1 1 1 2 1 2 2 Batch Y0000632 Calcitonin-Gly C0200010 N-acetyl-cys1-calcitonin C0225000 Calcitriol Buprenorphine - reference spectrum Buprenorphine hydrochloride - reference spectrum Buserelin Buserelin - Reference spectrum D-His-Buserelin Buspirone hydrochloride Buspirone for system suitability Busulfan Butyl parahydroxybenzoate Butylhydroxyanisole Butylhydroxytoluene Bumetanide Bumetanide impurity A Bumetanide impurity B Bupivacaine hydrochloride Bupivacaine impurity B Bupivacaine impurity E B1160490 B1160500 B1168000 Y0000357 B1168020 Y0000131 Y0000471 B1170000 B1217000 B1212000 B1215000 B1158000 Y0000309 Y0000310 B1160000 Y0000088 New Y0000089 Order Reference Standard Code B1156000 Bufexamac B1157400 Buflomedil hydrochloride B1157410 Buflomedil impurity B Catalogue No. 48-2006/4 n/a n/a 125 mg 0.4 ml 0.1 mg 10 mg 100 mg 100 mg 5 mg n/a n/a 5 mg n/a 0.98 mg n/a n/a 4.92 mg n/a 0.5 mg 5 mg 2 mg 50 mg 50 mg 50 mg 50 mg 150 mg 5 mg 5 mg 100 mg 20 mg 20 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 7 84.6% CœÕHœŒCaNŸOŸ 0.98 mg per vial of CŒ÷—Hœ÷ÕN÷÷O÷‡Sœ ; Batch 6 is valid until 31 October 2006 About 0.9 mg per ml Batch 2 is valid until 31 March 2006 100.0% CœŸH÷÷O– ; Batch 5 is valid until 28 February 2007 Batch 4 is valid until 31 December 2005 93.9% CœŸH÷ÕO– 95.6% CœŸH÷÷Oœ 99.8% CœÿH–ŸN—Oœ Plastic additive 07 4.92 mg per vial of CÿÕH‡ÿNŒÿOŒ– (2RS)-N-(2,6-dimethylphenyl)piperidine-2-carboxamide 6-(butylamino)-N-(2,6-dimethylphenyl)hexanamide ; Batch 1 is valid until 30 April 2007 3-nitro-4-phenoxy-5-sulphamoylbenzoic acid 3-amino-4-phenoxy-5-sulphamoylbenzoic acid Information Unit Sale Quantity Unit 100 mg 1 100 mg 1 20 mg 1 4-(pyrrolidin-1-yl)-1-(4-hydroxy-2,6-dimethoxyphenyl)butan-1one Yes +5°C -20°C -20°C -20°C -20°C +5°C -20°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage l l a c c c c g c l l f l c l l c l c g g a a a a a a a g g G 79 79 79 1000 79 79 79 79 79 79 79 150 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a For extra charges please see 2.2 0883 1182 0978,1606 0471 0471 0883 1180 1181 1077 1077 1077 1711 1711 0542 0881, 1216 0880 0581,30103,30105, 30106,30107 1773 0267,0268 1295 1295 2011 2011,2284 2284 0471 1076 1076 1076 0541 0541 0541 1179 1398 1398 Monograph 6 December 2006 1 1 3 1 3 1 1 2 1 3 5 Calcium levulinate dihydrate Calcium oxalate monohydrate Calcium pantothenate Camphor (racemic) Canrenone Caprylic acid Capsaicin Captopril Carbachol Carbamazepine Carbamazepine impurity A Carbasalate calcium - reference spectrum Carbenicillin sodium Carbidopa Carbimazole Carbocisteine Carbon dioxide - reference spectrum Carboplatin - reference spectrum Carboprost trometamol Carboprost trometamol - reference spectrum Carisoprodol Carisoprodol impurity A Carmustine - reference spectrum Carmustine impurity A Carteolol hydrochloride - reference spectrum Carteolol for system suitability Carvedilol - reference spectrum Carvedilol impurity C C0340000 C0350000 C0400000 C0405000 C0410000 C0426000 Y0000671 C0430000 Y0000113 C0450000 Y0000033 C0451000 C0455000 C0460000 C0465000 C0470000 C0499900 C0550000 Y0000475 Y0000536 Y0000035 Y0000036 C0580004 C0580010 Y0000192 Y0000193 Y0000075 Y0000103 2 C0630000 Cefaclor © Council of Europe, all rights reserved 2006 2 C0600000 Casein BRP n/a 1 n/a 1 n/a 1 n/a 2 1 1 1 n/a n/a 1 n/a 1 1 1 1 Batch Order Reference Standard Code C0299000 Calcium glucoheptonate C0300000 Calcium gluconate Catalogue No. 48-2006/4 100000 mg 450 mg n/a 20 mg n/a 30 mg n/a 10 mg n/a 50 mg 50 mg 100 mg 50 mg n/a n/a 40 mg n/a 50 mg 10 mg 250 mg 500 mg 60 mg 50 mg 50 mg 200 mg 50 mg 10 mg 50 mg 200 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Information 8 95.0% CŒ—HŒ÷ClN–O÷S (2RS)-1-[benzyl[2-(2-methoxyphenoxy)ethyl]amino]-3-(9Hcarbazol-4-yloxy)propan-2-ol 1,3-bis(2-chloroethyl)urea (2RS)-2-(hydroxymethyl)-2-methylpentyl(1-methylethyl)carbamate 99.9% CŒ—HŒœNœO ; Batch 2 is valid until 31 August 2006 10,11-dihydro-5H-dibenz[b,f]azepine-5-carboxamide (10,11-dihydrocarbamazepine) ; Batch 4 is valid until 28 February 2007 Batch 3 is valid until 30 June 2006 98.6 % CŒ‡HœŸNO– Batch 2 is valid until 31 May 2006 Loss of 12.1% m/m Batch 2 is valid until 31 July 2006 Unit Sale Quantity Unit 60 mg 1 100 mg 1 Calcium digluconate 0986 0350 1187 1187 1972 1972 1745 1745 1185 812,956 0755 0884 0885 0375 1081 1712 1712 1689 1689 Yes Yes +5°C +5°C +5°C +5°C -20°C +5°C +5°C -20°C +4°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c a l c l a l a a a a l l c l a a l a a a a a a g a a a a 79 131 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 1399 0172,0658,0979, 1047,1399 1296 20234 0470 0655 0688 1401,1471 1859,2336,2337 1079 1971 0543 0543 Monograph 6 December 2006 Delta-3-Cefaclor Cefadroxil Cefalexin monohydrate Cefalotin sodium Cefalotin for impurity B identification Cefamandole nafate Reference Standard 3 3 2 2 1 1 1 n/a C0691000 Ceftriaxone sodium C0692000 Ceftriaxone impurity A C0694990 Cefuroxime axetil C0695000 Cefuroxime sodium Y0000311 Celiprolol hydrochloride Y0000312 Celiprolol impurity I Y0000239 Celiprolol for peak identification C0698000 Cellulose acetate - reference spectrum © Council of Europe, all rights reserved 2006 2 1 1 2 1 n/a 1 4 1 2 3 1 1 2 Cefazolin Cefepime dihydrochloride monohydrate Cefepime dihydrochloride monohydrate for system suitability Cefixime Cefoperazone dihydrate Cefoperazone sodium - reference spectrum Cefotaxime acid Cefotaxime sodium Cefotaxime sodium for peak identification Cefoxitin sodium Cefradine 1 1 1 2 2 2 2 1 1 Batch Y0000568 Cefradine for peak identification C0690500 Ceftazidime C0690510 Ceftazidime impurity A C0682800 Y0000633 Y0000634 C0684000 C0684750 C0684800 Y0000420 New C0685000 Y0000506 C0688000 C0690000 Y0000240 Cefapirin sodium C0682400 Cefatrizine propylene glycol C0682410 Cefatrizine impurity A Order Code C0640000 C0650000 C0675000 C0682000 Y0000505 C0682300 Catalogue No. 48-2006/4 80 mg 10 mg 60 mg 150 mg 10 mg 0.02 mg 20 mg n/a 6 mg 200 mg 15 mg 15 mg 200 mg 100 mg n/a 80 mg 30 mg 10 mg 250 mg 300 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 9 1-acetyl-1-(4-ethoxyphenyl)-3,3-diethylurea 85.5% CœœHœœNÿOŸSœ 83.1% CœœHœœNÿOŸSœ; (6R,7R)-7-[[(Z)-2-(2-aminothiazol-4-yl)-2-[(1-carboxy-1-methyl ethoxy)imino]acetyl]amino]-8-oxo-3-[(1-pyridinio)-methyl]-5thia-1-azabicyclo[4.2.0]oct-3-ene-2-carboxylate (delta-2-ceftazidime) ; Batch 1 is valid until 30 June 2006 90.4% CŒ‡HŒÿN‡NaœOŸS– ; Batch 2 is valid until 31 August 2006 E-isomer 96.9% CœÕHœœN÷OŒÕS 96.6% CŒÿHŒ—N÷NaO‡S 98.4% CŒÿHŒÿN–NaOŸSœ 94.2% CŒÿHŒ„N–O÷S (Cefradine) 1.8% CŒÿHŒŸN–O÷S (Cefalexin) 94.3% CŒÿHŒŸN—OŸSœ Batch 3 is valid until 31 May 2007 88.4% CŒÿHŒ—N—OŸSœ 93.6% Cœ—HœŸN„O‡Sœ Information Unit Sale Quantity Unit 30 mg 1 250 mg 1 93.7% CŒÿHŒŸN–O—S 150 mg 1 94.1% CŒÿHŒŸN–O÷S 100 mg 1 98.8% CŒÿHŒ—NœNaOÿSœ 10 mg 1 125 mg 1 94.4% CŒ„HŒŸNÿNaOÿSœ (cefamandole nafate) corresponding to: 85.2% CŒ‡HŒ‡NÿO—Sœ (cefamandole) 4.4% CŒ‡HŒ‡NÿO—Sœ (cefamandole free acid) 100 mg 1 98.5% CŒŸHŒÿN–NaOÿSœ 150 mg 1 81.8% CŒ‡HŒ‡NÿO—Sœ 60 mg 1 7-amino-(6R,7R)-3-[(2H-1,2,3-triazol-4-yl)sulfanyl]-methyl-8oxo-5-thia-1-azabicyclo[4.2.0]oct-2-ene-2-carboxylic acid (7-ACA triazole) 150 mg 1 99.4% CŒ÷HŒ÷N‡O÷S– 150 mg 1 95.2% CŒ„HœÿClœNÿO—Sœ Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a c a l a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 c 79 a 79 a 79 a 79 a 79 a 0991 +5°C a 0991 +5°C a 1300 +5°C a 0988,0992 +5°C a 1632 +5°C a 1632 +5°C a 1632 Yes +5°C a 0887 l For extra charges please see 2.2 0988 2126 2126 1188 1404 1404 0989 0708,0989 0989 0990 0167,0168,0578, 0708,0814 0814 1405 1405 1650 1403 1403 0986 0260,0577,0813 0708 0987 0987 1402 Monograph 6 December 2006 Cetyl palmitate 15 Cetyl palmitate 95 Cetylpyridinium chloride Chenodeoxycholic acid Chitosan hydrochloride Chlorambucil Chloramphenicol Chloramphenicol dipalmitate Chloramphenicol disodium disuccinate Chloramphenicol palmitate isomer Chloramphenicol sodium succinate Chlorcyclizine hydrochloride Chlordiazepoxide - * psy Chlordiazepoxide hydrochloride - * psy Chlordiazepoxide impurity A Chlorhexidine Chlorhexidine diacetate Chlorhexidine dihydrochloride Chlorhexidine for performance test Chlorogenic acid Chloromethylnitroimidazole (2-Chlorophenyl)diphenylmethanol 1-(4-Chlorophenyl)-1-phenylethanol Chloroquine sulphate Chlorothiazide Chlorphenamine maleate Y0000073 Y0000074 C1000000 C1050000 Y0000104 C1100000 C1200000 C1300000 C1350000 C1400000 C1425000 C1435000 C1450000 C1500000 Y0000476 C1510000 C1520000 C1540000 C1530000 Y0000569 C1600000 C1605000 C2223030 C1650000 C1700000 C1800000 © Council of Europe, all rights reserved 2006 3 3 n/a 1 Cetirizine dihydrochloride Cetirizine impurity A Cetostearyl isononanoate - reference spectrum Cetyl alcohol C0980650 C0980651 C0984100 C0990000 1 5 1 3 1 1 4 2 1 4 1 1 1 1 1 1 1 2 1 3 1 1 1 1 1 1 n/a n/a 2 Batch Order Reference Standard Code C0698005 Cellulose acetate butyrate - reference spectrum C0698020 Cellulose acetate phthalate - reference spectrum C0700000 Cephaëline hydrochloride Catalogue No. 48-2006/4 100 mg 20 mg 20 mg 200 mg 100 mg 100 mg 50 mg 10 mg 50 mg 30 mg 20 mg 60 mg 50 mg 50 mg 125 mg 30 mg 100 mg 500 mg 100 mg 25 mg 100 mg 1500 mg 100 mg 50 mg 100 mg 10 mg 100 mg 10 mg n/a 250 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 Unit Sale Quantity Unit n/a 1 n/a 1 10 mg 1 10 Batch 4 is valid until 31 January 2006 Clemastine fumarate impurity C Batch 2 is valid until 31 July 2006 96.9% CŒÿHŒ‡O„ Batch 1 is valid until 28 February 2006 7-chloro-5-phenyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one 4-oxide 91.1% CŒ„HŒ‡ClœNœNaœOŒŒ 100% CŒÿH–÷O (RS)-1-[(4-chlorophenyl)phenylmethyl]piperazine Information Yes +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a c a a a g g a a a a a a a a g a a a a a a j j a a a l a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 l 79 l 79 a For extra charges please see 2.2 0658 0657 0659 0657,0658,0659 0897,1823,1824, 1866 0369 0757 1190 0544,0545 0385,0394 0386,0977,1084, 1196 1406 0314 0080,0081,0093, 0094,1530,1875 1084 1084 1085 0540,0702,0801, 0802,0847,0969, 1411 1906 1906 0379 1189,1275 1774 0137 0071,0473,0709 0473 0709 0473 0709 1086 0656,1974 0474 0474,0656 Monograph 6 December 2006 1 1 1 1 4 1 5 4 6 4 Y0000479 Chlorpromazine impurity D Chlorpromazine impurity E Chlorpropamide Chlorpropamide impurity B Chlorprothixene hydrochloride Chlortalidone Chlortalidone impurity B Y0000508 C1905000 C1905020 C1915000 C1950000 C1950020 C2000000 Chlortetracycline hydrochloride C2100000 Cholecalciferol C2150000 Cholecalciferol for performance test Ciclopirox impurity B Ciclopirox olamine Ciclosporin Ciclosporin for system suitability Cilastatin sodium Cilazapril © Council of Europe, all rights reserved 2006 C2162702 C2162700 C2163000 Y0000361 C2170000 C2174000 2 1 2 1 2 1 2 1 1 1 2 1 1 1 1 2 1 1 C1900000 Chlorpromazine hydrochloride Y0000507 Chlorpromazine impurity A Cholesterol Cholic acid Chondroitin sulphate sodium Chondroitin sulphate sodium (marine) Chymotrypsin BRP Cladribine Cladribine for peak identification Cladribine impurity C Ciclopirox Ciclopirox impurity A 1 Y0000437 Chlorphenamine impurity C C2155000 C2158000 Y0000280 Y0000593 C2160000 New Y0000639 New Y0000609 New Y0000610 Y0000040 C2162701 1 Batch Order Reference Standard Code Y0000436 Chlorphenamine impurity A Catalogue No. 48-2006/4 20 mg 150 mg 120 mg 5 mg 10 mg 50 mg 60 mg 60 mg 250 mg 100 mg 100 mg 50 mg 10 mg 5 mg 100 mg 20 mg 1 ml 500 mg 100 mg 10 mg 100 mg 50 mg 50 mg 50 mg 10 mg 10 mg 200 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0475 1087 1087 0815,1365 0546 0546 0475 0475,20303 0475 0386 0386 Monograph 11 98.8% CÿœHŒŒŒNŒŒOŒœ 1302 0994 0994 1408 1499 Yes Yes -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c g a a a a a a a a a b b b a a c c a a a a g a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 2-(4-chloro-3-sulfamoylbenzoyl)benzoic acid ; Batch 4 is valid until 31 December 2005 89.7% CœœHœ÷ClœNœO‡ 0173 5.5% Cœ—Hœ—ClNœO‡ 100% CœŸH÷÷O; Vitamin D3 ; Batch 5 is valid until 28 February 2007 0072,0574,0575, 0598,1192,1193 0072,0082,0574, 0575,0598 99.2% CœŸH÷ÿO 0993 1189,1275 100% HœO(CŒ÷HŒ„NNaœOŒ÷S)¨ 2064 2064 6.01 microkatals per mg 0476,0694 99.1% CŒÕHŒœClN—O– 2174 2174 2-chloro-7H-purin-6-amine 21-74 1407 (¢£)-2-(3-cyclohexyl-5-methyl-4,5-dihydroisoxazol-5-yl)acetic 1302,1407 acid 6-cyclohexyl-4-methyl-2§-pyran-2-one 1302,1407 1,3-Dipropylurea 2.0% E-isomer 3-(2-chloro-10H-phenothiazin-10-yl)-N,N-dimethylpropan-1amine S-oxide (chlorpromazine sulphoxide) 3-(2-chloro-10H-phenothiazin-10-yl)-N-methypropan-1-amine (demethylchlorpromazine) 2-chloro-10H-phenothiazine Information Unit Sale Quantity Unit 10 mg 1 2-(4-chlorophenyl)-4-(dimethylamino)-2-[2-(dimethylamino) ethyl]butanenitrile 10 mg 1 (3RS)-3-(4-chlorophenyl)-N-methyl-3-(pyridin-2-yl)propan-1amine 6 December 2006 1 1 1 1 1 1 1 1 3 1 4 Cimetidine Cimetidine hydrochloride Cinchocaine hydrochloride Cineole Cinnarizine Ciprofibrate Ciprofibrate for system suitability Ciprofloxacin Ciprofloxacin hydrochloride Ciprofloxacin hydrochloride for peak identification Ciprofloxacin impurity A Cisapride monohydrate Cisapride tartrate Cisplatin Citric acid (anhydrous) Citric acid monohydrate Clarithromycin Clarithromycin for peak identification Clazuril for system suitability Clazuril for veterinary use - reference spectrum Clebopride malate Clemastine fumarate Clenbuterol hydrochloride Clenbuterol impurity B Clindamycin hydrochloride Clindamycin phosphate Clioquinol Clobazam - reference spectrum Clobazam impurity A C2175000 C2175500 C2177000 Y0000176 C2180000 Y0000362 Y0000363 Y0000198 C2190000 Y0000199 C2190050 C2205000 C2205100 C2210000 A1202000 C2219000 Y0000320 Y0000321 Y0000269 Y0000262 C2221000 C2223000 C2248000 C2248010 C2250000 C2269000 Y0000364 Y0000205 Y0000241 © Council of Europe, all rights reserved 2006 1 C2174005 Cilazapril impurity D 3 2 1 n/a 1 1 1 2 1 1 2 1 1 n/a 1 1 1 1 1 Batch Order Reference Standard Code C2174002 Cilazapril impurity A Catalogue No. 48-2006/4 200 mg 250 mg 5 mg n/a 10 mg 30 mg 100 mg 150 mg 50 mg 50 mg 160 mg 30 mg 10 mg n/a 100 mg 100 mg 50 mg 20 mg 50 mg 100 mg 60 mg 180 mg 100 mg 5 mg 5 mg 20 mg 100 mg 10 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 12 7-chloro-5-phenyl-1,5-dihydro-1,5-dihydro-3H-1,5-benzodiazepine-2,4-dione 1-(4-amino-3,5-dichlorophenyl)-2-[(1,1-dimethylethyl)amino] ethanone (clenbuterol ketone) 93.3% CŒ‡H–÷ClœNœO—S 95.7% CŒ‡H–÷ClNœO‡PS ; Batch 1 is valid until 31 January 2006 97.5% C–‡Hÿ„NOŒ– ; Batch 1 is valid until 30 November 2006 100% [PtClœ(NH–)œ] Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a g l a a a g a a a a a l a a a a a a a g a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0582,0583,0996 0996 2111 1974 1974 0995 1503 0599 0455 0456 1651 1651 1714 1714 1303 1190 1409 1409 0756 1500 1088 1973 0816 2013 2013 1089 93.6% CŒŸHŒ„ClFN–O– 0888,1353 0888,1089 7-chloro-1-cyclopropyl-6-fluoro-1,4-dihydro-4-oxo-quinoline-3- 0888,1089 carboxylic acid (fluoroquinolonic acid) ; Batch 3 is valid until 30 April 2006 Information Unit Sale Monograph Quantity Unit 25 mg 1 1,1-dimethylethyl(1S,9S)-9-[[(S)-1-ethoxycarbonyl-3-phenylpro 1499 pyl]amino]-10-oxo-octahydro-6H-pyridazino[1,2a][1,2]diazepine -1-caboxylate 25 mg 1 (1S,9S)-9-[[(R)-1-ethoxycarbonyl-3-phenylpropyl]amino]-101499 oxo-octahydro-6H-pyridazino[1,2a][1,2]diazepine-1-carboxylic acid 6 December 2006 Clozapine Cocaine hydrochloride - reference spectrum Cocoyl caprylocaprate Codeine - reference spectrum Codeine impurity A (methylcodeine) © Council of Europe, all rights reserved 2006 1 n/a 1 n/a 2 2 3 1 1 1 C2460000 Y0000162 C2480000 C2500000 Y0000334 C2430000 C2450000 C2425600 C2424500 C2424550 1 1 1 1 n/a 1 1 1 1 Clomipramine impurity F Clonazepam - * psy Clonazepam impurity A Clonazepam impurity B Clonazepam - reference spectrum Clonidine hydrochloride Closantel sodium dihydrate Closantel for system suitability Clostridia (multi-component) rabbit antiserum(for vaccines-vet.use)BRP Clostridium tetani guinea pig antiserum (for vaccines human use) BRP Clostridium tetani guinea pig antiserum (for vaccines - vet. use) BRP Clostridium tetani rabbit antiserum (for vaccines - vet. use) BRP Clotrimazole Cloxacillin sodium Y0000134 C2385000 C2385010 C2385015 Y0000286 C2400000 Y0000392 Y0000393 C2424400 1 1 1 1 1 1 1 2 1 1 1 Batch 1 Clobetasol propionate Clobetasol for peak identification Clobetasol impurity J Clobetasone butyrate Clofazimine Clofazimine for system suitability Clofibrate Clomifene citrate Clomifene citrate for performance test Clomipramine hydrochloride Clomipramine impurity C Reference Standard Y0000133 Clomipramine impurity D Order Code Y0000559 Y0000570 Y0000571 C2285000 Y0000313 Y0000358 C2300000 C2320000 C2332000 C2360000 Y0000132 Catalogue No. 48-2006/4 60 mg n/a 40 mg n/a 10 mg 100 mg 125 mg 1 mg 1 mg 1 mg 50 mg 25 mg 25 mg n/a 100 mg 20 mg 20 mg 1 mg 1 1 1 1 1 1 1 1 1 3 1 1 1 1 1 1 1 1 13 7,8-didehydro-4,5 ¶-epoxy-3,6 ¶-dimethoxy-17-methylmorphinan Yes Yes Yes Yes Yes Yes Yes Yes -20°C -20°C -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c c c a j a a l a a a c a 79 79 79 79 79 79 79 90 90 90 90 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 0757 +5°C g 0661,0663,0668, +5°C a 2260 1191 +5°C g 0073 l 1411 +5°C a 0074,0075,0076 l 0074,0075,0076, +5°C a 1412 For extra charges please see 2.2 See leaflet,0697 15 IU per vial 94.6% CŒ„HŒŸClN–NaO—S See leaflet,0697 0889 1974 0890 0890 0890 0477 1716 1716 0362,0363,0364, 0697 20708 0889 2127 2127 2127 1090 2054 2054 0318 0997,1046 0997 0889 0889 Monograph 34 IU per vial 0.20 IU per vial (determined using toxin neutralisation test) see information on the accompanying leaflet 2-Amino-2'-chloro-5-nitrobenzophenone 3-Amino-4-(2-chlorophenyl)-6-nitro-1§-quinolin-2-one Information Unit Sale Quantity Unit 40 mg 1 99.6% Cœ—H–œClFO— 2 mg 1 0.4 mg 1 50 mg 1 150 mg 1 10 mg 1 0.5 ml 1 50 mg 1 44% of Z-isomer ; Batch 1 is valid until 31 December 2006 50 mg 1 100 mg 1 10 mg 1 94.5% Clomipramine impurity C; 3-(3-chloro-5H-dibenzo[b,f]azepin-5-yl)-N,N-dimethylpropan-1amine 10 mg 1 3-(3,7-dichloro-10,11-dihydro-5H-dibenzo[b,f]azepin-5-yl)-N,Ndimethylpropan-1-amine 5 mg 1 3-chloro-10,11-dihydro-5H-dibenzo[b,f]azepine 6 December 2006 Colistin sulphate for microbiological assay Copovidone - reference spectrum Cortisone acetate Coumarin Cotton wool. standard for neps Crospovidone - reference spectrum Crotamiton Crotamiton impurity A Cyanocobalamin C2700000 C2725000 C2800000 Y0000438 C2900000 C2950000 C2970000 C2970005 C3000000 C3090000 Cyclizine hydrochloride C3200000 Cyclobenzaprine hydrochloride C3230000 Cyclohexa-1,4-dienylglycine C3245000 Cyclopentolate hydrochloride C3250000 Cyclophosphamide C3280000 Cyproheptadine hydrochloride C3283000 Cyproterone acetate C3290000 Cysteine hydrochloride monohydrate C3300000 Cystine C3350000 Cytarabine D0070000 Dalteparin sodium Y0000600 Danaparoid sodium D0100000 Dapsone D0125000 Daunorubicin hydrochloride D0120000 Daunorubicinone D0160000 Deferoxamine mesilate D0201000 Dehydrohexetidine Y0000611 Dembrexine hydrochloride monohydrate D0300000 Demeclocycline hydrochloride © Council of Europe, all rights reserved 2006 Codeine hydrochloride dihydrate - reference spectrum Codergocrine mesilate Colchicine Colchicine for system suitability Colestyramine Colistimethate sodium Colistin sulphate (for LC assay) Reference Standard Order Code C2500100 C2510000 C2580000 Y0000209 Y0000374 C2600000 Y0000277 Catalogue No. 48-2006/4 1 1 1 1 1 1 2 1 1 1 2 1 2 3 2 2 1 1 4 n/a 1 2 4 2 n/a 5 1 1 n/a 1 1 1 1 1 3 Batch 50 mg 100 mg 80 mg 60 mg 50 mg 30 mg 30 mg 50 mg 100 mg 150 mg 250 mg 200 mg 100 mg 100 mg 10 mg 30 mg 50 mg 10 mg 100 mg n/a 100 mg 30 mg 20 mg n/a 250 mg 80 mg 1000 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 92.4% CœŒHœœClœNœO‡ 14 98.0% CœŸH–ÕClNOŒÕ Daunorubicin aglycone Batch 1 is valid until 30 April 2006 Batch 1 is valid until 30 September 2006 98.9%CŒ–HŒŸNO(sum of E and Z-isomers); 2.9% Z-isomers N-ethyl-N-(2-methylphenyl)but-3-enamide Vitamin B12 ; Batch 3 is valid until 31 July 2006 99.9% C„HÿOœ Information Unit Sale Quantity Unit n/a 1 60 mg 1 50 mg 1 50 mg 1 10 mg 1 100 mg 1 12850 IU per mg 25 mg 1 33.7% colistin E2, 2.6% colistin E3, 3.3% colistin E1-I, 3.1% colistin E1-7MOA, 44.2 % colistin E1. 25.0 mg of colistin sulphate per vial 25 mg 1 576 000 IU per vial; For microbiological assay only Yes Yes +5°C +5°C Room temp. -20° C +5°C +5°C +5°C +5°C +5°C -20°C Leaflet Storage a l a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 l 79 a 79 a 79 a 79 a 79 a 79 a 0892 l 1194 -20°C c 1194 -20°C c 0269,0270,0547, +5°C a 0710,1505 1092 +5°C a 0408,0464 +5°C a 0814 +5°C a 1093 +5°C a 0711 +5°C a 0817,0846 +5°C a 1094 +5°C g 0895 +5°C a 0998 +5°C a 0760 +5°C a 0828 +5°C a 2090 +5°C b 0077 +5°C a 0662 +5°C a 0662 +5°C a 0896 -20°C a 1221 +5°C a 2169 +5°C a 0176 +5°C a For extra charges please see 2.2 0891 0321,0736,0767 2120 0036 1412 1416,2060 0758 0758 1775 0319,20702 0320 Monograph 6 December 2006 1 1 1 3 1 3 1 1 Dexamethasone isonicotinate Dexamethasone isonicotinate for impurity C identification Dexamethasone pivalate Dexamethasone sodium phosphate Dexchlorpheniramine maleate Dexpanthenol Dextran Dextran 1 Dextran Vo Dextran 4 for calibration Dextran 10 for calibration Dextran 40 for calibration Dextran 70 for calibration Dextran 250 for calibration Y0000538 Y0000511 D0718000 D0720000 D0720800 D0730000 D0731000 D0731005 D0732000 D0733000 D0734000 D0735000 D0736000 D0737000 © Council of Europe, all rights reserved 2006 2 D0710000 Dexamethasone acetate 1 1 1 1 1 1 1 1 4 Y0000001 Detomidine hydrochloride D0660020 Detomidine impurity B New D0700000 Dexamethasone Y0000509 Desogestrel Y0000510 Desogestrel for system suitability D0400000 Desoxycortone acetate 1 1 1 n/a 4 1 1 1 1 1 2 1 6 Y0000228 D0406000 D0406200 D0430000 D0431000 D0480000 D0500000 D0600000 D0630000 D0650000 Demethylflumazenil - reference spectrum Deoxyminoxidil Deptropine citrate Dequalinium chloride Dequalinium chloride for performance test Desacetylvinblastine Desipramine hydrochloride Deslanoside Desmethylmetrifonate Desmopressin 2 Batch Order Reference Standard Code D0350000 N-Demethylerythromycin A Catalogue No. 48-2006/4 10 mg 50 mg 50 mg 50 mg 50 mg 50 mg 10 mg 10 mg 50 mg 50 mg 60 mg 5 mg 25 mg 50 mg 100 mg 100 mg 20 mg 60 mg 50 mg 10 mg 250 mg n/a 0.25 mg 60 mg 50 mg 50 mg 1 mg 100 mg 150 mg 30 mg 0.98 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 M™´¨ M™´¨ M™´¨ M™´¨ M™´¨ 15 3050-Mö 3850 88000 - Mö 10450 30500- Mö 40900 58900- Mö 70300 121800- Mö 238200 Average molecule mass : 930-1000 Fraction with less than 3 glucose units : 8.0 to 10.5% Fraction with more than 9 glucose units : 10.0 to 12.5% (RS)-(1-benzyl-1H-imidazol-5-yl)(2,3-dimethylphenyl)methanol Batch 3 is valid until 30 April 2007 0.98 mg per vial of C÷ÿHÿ÷NŒ÷OŒœS ; Batch 5 is valid until 30 November 2006 99.9% CœœH–ÕO 98.8% C÷ŸHŸ÷OŒ„ Information Unit Sale Quantity Unit 10 mg 1 Batch 1 is valid until 31 March 2006 20239 20239 20239 20239 20239 20239 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C -20°C +5°C Leaflet Storage a a a a a a a a a a a a a a a a a a a a a l a a a a c a a a c 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 1717 1717 0322,0809,0850, 1327 1414 1414 0312,0388,0768, 1376,2237 0548,0933,0975, 2237 2237 2237 1327 0549,0735,0810 1196 0761 0999,1000,1001 1506 0179,0274,0490, 0552,1098 1917 0937 1308 1413 1413 1276 0481 0482 1133 0712 Monograph 6 December 2006 Dienestrol Diethanolamine fusidate Diethylcarbamazine citrate Diethylene glycol (monoethyl ether) - reference spectrum Diethyl phthalate Diethylstilbestrol Diethylstilbestrol dimethyl ether Diethylstilbestrol monomethyl ether Diflunisal Digitoxin Digoxigenin Digoxin Digoxin for peak identification D1200000 D1250000 D1300000 Y0000217 D1410000 D1500000 D1600000 D1700000 D1750000 D1800000 Y0000640 D1900000 Y0000554 © Council of Europe, all rights reserved 2006 Dextran 40 for performance test Dextran 60/70 for performance test Dextromethorphan hydrobromide Dextromethorphan impurity A Dextropropoxyphene hydrochloride - reference spectrum Diazepam - * psy Diazepam for system suitability - * psy Diazoxide Dibenzocycloheptene Dibenzosuberone Dibrompropamidine diisetionate Dibrompropamidine for system suitability Dibutyl phthalate Dichlorodiaminocyclohexaneplatinum Diclazuril for system suitability Diclazuril for veterinary use - reference spectrum Diclofenac potassium Diclofenac impurity A Dicloxacillin sodium Dicycloverine hydrochloride Didanosine Didanosine for system suitability Didanosine impurity A Didanosine impurity G Reference Standard Order Code D0738000 D0739000 D0740000 Y0000261 D0750000 D0940000 Y0000596 D0950000 D0970000 D1000000 Y0000480 Y0000481 D1010000 New Y0000275 Y0000259 Y0000264 D1039990 D1040000 D1050000 D1060000 Y0000439 Y0000440 Y0000441 Y0000442 Catalogue No. 48-2006/4 3 1 1 n/a 1 1 1 1 1 2 1 7 1 1 1 3 1 n/a 1 1 1 2 1 1 1 1 2 1 n/a 2 3 3 1 1 1 1 1 Batch 50 mg 250 mg n/a 1 ml 100 mg 10 mg 10 mg 30 mg 250 mg 5 mg 30 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 16 98.5% C÷ŒHÿ÷OŒ÷ ; Batch 6 is valid until 30 June 2006 99.0% C÷ŒHÿ÷OŒ– 100% CŒ‡HœÕOœ. Dried at 100-105°C for 2 h Information Unit Sale Quantity Unit 50 mg 1 50 mg 1 100 mg 1 Batch 2 is valid until 30 April 2006 5 mg 1 (S,13S,14S)-3-methoxymorphinan n/a 1 30 mg 1 0.5 mg 1 50 mg 1 20 mg 1 100 mg 1 10 mg 1 20 mg 1 1 ml 1 10 mg 1 Batch 1 is valid until 30 April 2007 20 mg 1 n/a 1 100 mg 1 5 mg 1 1-(2,6-dichlorophenyl)indolin-2-one 250 mg 1 93.7% CŒ„HŒÿClœN–NaO—S 100 mg 1 10 mg 1 10 mg 1 10 mg 1 1,7-dihydro-6H-purin-6-one (hypoxanthine) 10 mg 1 9-(2,3-dideoxy-ß-D-glycero-pentofuranosyl)-9H-purin-6-amine (2',3'-dideoxyadenosine) 150 mg 1 100% CŒ‡HŒ‡Oœ Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a g l a a a a a a f f f 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 g 79 g 79 l 79 j 79 j 79 a 79 a 79 a 79 a 79 a 79 a 79 g 79 a 79 l 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a For extra charges please see 2.2 0483,0484 0798,0848 0271 1198 0897 0483,0484 0484 0484 0818,0864 0078,0079,0117 0079 0079 0079 20239 20239 0020 0020 0713 0022 0022 0550 0817 0464,0941 2300 2300 0762 2017 1718 1718 1508 1002,1281,1508 0661,0663,0668 1197 2200 2200 2200 2200 Monograph 6 December 2006 Dihydrotachysterol Dihydrotachysterol for system suitability Diltiazem hydrochloride Diltiazem impurity A Dimenhydrinate (2,6-Dimethylphenoxy)acetone N,N-Dimethylacetamide - reference spectrum Dimethyl sulfoxide Dimeticone Dimetindene maleate Dinoprost trometamol Dinoprostone Dinoprostone impurity C Diosmin Diosmin for system suitability Diphenhydramine hydrochloride Diphenhydramine impurity A Diphenoxylate hydrochloride - reference spectrum Diphtheria toxin BRP - * Biotox Y0000544 Y0000482 D1980000 D1982000 D2000000 D2046000 Y0000234 D2050000 D2200000 D2205000 D2255000 D2250000 D2250015 Y0000094 Y0000095 D2600000 Y0000135 D2630000 Y0000258 D2700000 Diphtheria vaccine (adsorbed) BRP Y0000376 Dipivefrine hydrochloride Y0000394 Dipivefrine for system suitability D2750100 Dipotassium clorazepate - reference spectrum © Council of Europe, all rights reserved 2006 Dihydralazine for system suitability Dihydralazine sulphate (hydrated) - reference spectrum Dihydrocodeine hydrogen tartrate - reference spectrum 17 alpha-dihydroequilin Dihydroergocristine mesilate Dihydroergotamine mesilate Dihydroergotamine tartrate Dihydrostreptomycin sulphate Reference Standard Order Code Y0000232 D1940001 Y0000216 Y0000053 D1945000 D1950000 D1952000 D1954000 Catalogue No. 48-2006/4 3 1 1 n/a 1 2 1 2 n/a 1 1 1 n/a 2 2 1 1 2 1 1 1 3 1 1 n/a n/a 1 1 3 2 n/a Batch 32 mg 100 mg 10 mg n/a 50 mg 5 mg 100 mg 10 mg n/a 1 ml 100 mg 50 mg n/a 1 ml 200 mg 50 mg 60 mg 100 mg 10 mg 5 mg 200 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1611 1611 0023,1190 0023 0819 See leaflet,0443 0601 1029 1667 0763 0138,1470 1417 1312 1311 1311,1488 2014 2014 1004,1199 1004 1310 1310 1776 1512 1416,2060 0551 0600 0485,20702 Monograph Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C -20°C +5°C +5°C +5°C -20°C +5°C Leaflet Storage a a a a l f a a l a a a c c a c c a a 79 79 79 90 90 79 79 79 79 79 240 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 l 79 l 79 c 79 a 79 a 79 a 79 a Nominal concentration of Diphtheria toxin: 1 Lf/ml (0.4μl/ml) Yes +5°C Systemic toxicity: 77.6 LD—Õ/ml (determined in the subcutaneous challenge test in guinea pigs) Maximum intradermal toxicity: 75,000Lr/Lf (determined in the guinea pig intradermal skin test) Toxicity in the Vero cell assay: concentrations of 5x10-Î Lf/ml and below cause cytotoxic effects. 160 IU per vial See leaflet,20706 Yes -20°C c 1719 +5°C g 1719 +5°C g 0898 l 17 For extra charges please see 2.2 2-(diphenylmethoxy)-N-methylethanamine 98.2% Cœ÷H÷—NO‡ 99.8% CœÕH–œO (E)-7-[(1S,2R,3R)-3-hydroxy-2-[(E)-(3S)-3-hydroxyoct-1-enyl]5-oxocyclopentyl]-hept-5-enoic acid (5-trans-PGEœ ; (5E)-PGEœ) 94.6% Cœ‡H–œOŒ— Batch 1 is valid until 30 April 2006 99.8% dimeticone (2¢,3£)-3-acetyloxy-5-[2-(dimethylamino)ethyl]-2-(4-methoxy phenyl)-2,3-dihydro-1,5-benzothiazepin-4(5§)-one Information Unit Sale Quantity Unit 10 mg 1 n/a 1 n/a 1 10 mg 1 98.2% CŒ‡HœœOœ 250 mg 1 100 mg 1 150 mg 1 100.0% CŸÕH‡ÕNŒÕOŒÿ. Dried at 100-105°C at constant weight 200 mg 1 820 IU per mg; International standard provided for an interim period 10 mg 1 100.0% Cœ‡H÷ÿO 6 December 2006 Diprophylline Dipyridamole Dirithromycin Disodium edetate Disopyramide Disopyramide phosphate Disulfiram Dithranol Dithranol impurity C Reference Standard 5 3 n/a D2975000 Doxorubicin hydrochloride D3000000 Doxycycline hyclate Y0000163 Doxylamine hydrogen succinate - reference spectrum © Council of Europe, all rights reserved 2006 1 1 1 n/a 2 2 Doxazosin mesilate Doxazosin impurity D Doxazosin impurity F Doxepin hydrochloride - reference spectrum Doxepin impurity A Doxepin impurity B Y0000553 Y0000551 Y0000552 D2964500 D2964510 D2964520 1 2 n/a 1 1 1 1 1 1 1 1 1 1 1 Dobutamine hydrochloride Docosahexaenoic acid ethyl ester Docusate sodium - reference spectrum Dodecyl gallate Domperidone Domperidone maleate Dopamine hydrochloride Dopexamine dihydrochloride Dopexamine impurity B Dopexamine impurity F Dosulepin hydrochloride Dosulepin impurity A 3 1 1 1 1 1 1 1 1 2 Batch D2963000 Doxapram hydrochloride Y0000208 Doxapram impurity B D2954000 D2954600 D2954500 Y0000365 D2955000 D2957000 D2960000 Y0000612 Y0000613 Y0000614 D2962000 D2962005 New D2953050 Dithranol impurity D Order Code D2800000 D2850000 D2880000 D2900000 D2920000 D2922000 D2950000 D2953000 D2953025 Catalogue No. 48-2006/4 150 mg 100 mg n/a 60 mg 10 mg 10 mg n/a 20 mg 25 mg 50 mg 10 mg 100 mg 150 mg n/a 30 mg 150 mg 150 mg 50 mg 10 mg 10 mg 10 mg 100 mg 50 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1201 1201 1200 2063,20429 1418 2078 1009 1008 0664,1200 1748 1748 1748 1314 1314 1007 0486 1199 1313 0232 1006 1005 0603 1007 1007 Monograph 18 1589 -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c a l a a a l a a a a a a l a a a a a c c a a g 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 g 79 g For extra charges please see 2.2 2125 2125 2125 1096 dibenzo[b,e]oxepin-11(6H)-one 1096 (11RS)-11-[3-(dimethylamino)propyl]-6,11-dihydrodibenzo[b,e] 1096 oxepin-11-ol 99.0% CœŸH–ÕClNOŒŒ 0714,0662,1590 85.6% CœœHœ÷NœO‡ 0272,0820 (4RS)-1-ethyl-4-[2-[(2-hydroxyethyl)amino]ethyl]-3,3-diphenylpyrolidin-2-one 99.2% Cœ÷Hœ„N—O‡S (E)-3-(6,11-dihydrodibenzo[b,e]thiepin-11-ylidene)-N,N'dimethylpropan-1-amine £-oxide 91.2% DHA ethyl ester Information Unit Sale Quantity Unit 100 mg 1 50 mg 1 100 mg 1 97.4% C÷œHŸ‡NœOŒ÷ 100 mg 1 100 mg 1 100 mg 1 100 mg 1 125 mg 1 20 mg 1 Dithranol-dimer 4,4',5,5'-tetrahydroxy-9,9'-bianthracenyl-10,10'(9H,9'H)-dione ; Batch 1 is valid until 31 May 2006 20 mg 1 94.9% CŒ÷HŒÕOœ; 1-hydroxyanthracen-9(10H)-one ; Batch 2 is valid until 31 March 2007 6 December 2006 n/a 1 1 n/a 1 2 n/a 2 1 1 Y0000249 Ebastine - reference spectrum Y0000247 Ebastine impurity C Y0000248 Ebastine impurity D Y0000270 Econazole - reference spectrum Y0000254 Econazole for system suitability E0050000 Econazole nitrate Y0000296 E0085000 Y0000537 Y0000512 4-Epianhydrotetracycline hydrochloride 4-Epichlortetracycline hydrochloride 4-Epidemeclocycline hydrochloride 6-Epidoxycycline hydrochloride 4-Epioxytetracycline Epirubicin hydrochloride Enalapril for system suitability Enalapril maleate Enalaprilat dihydrate Enalaprilat for system suitability Enalaprilat impurity G Enilconazole Enilconazole impurity E Endotoxin standard BRP Enoxaparin sodium Enoxolone Enterokinase BRP Ephedrine hydrochloride (racemic) - * Drug Precursor Ephedrine hydrochloride - * Drug Precursor © Council of Europe, all rights reserved 2006 E0400000 E0430000 E0440000 E0500000 E0530000 E0550000 E0110000 E0109000 Y0000615 Y0000629 New Y0000678 Y0000136 Y0000137 E0150000 E0180000 E0180500 E0200000 E0305000 E0300000 E0100000 Emetine hydrochloride 4 3 1 4 6 4 1 2 1 1 1 1 1 4 3 1 1 1 1 1 1 D3100000 Droperidol Econazole nitrate - reference spectrum Eicosapentaenoic acid ethyl ester Emedastine difumarate Emedastine impurity E 1 Batch Order Reference Standard Code Y0000160 Doxylamine impurity A Catalogue No. 48-2006/4 10 mg 20 mg 20 mg 50 mg 40 mg 100 mg 20 mg 50 mg 100 mg 10 mg 0.005 mg 60 mg 20 mg 11 mg 200 mg 100 mg 500 mg 50 mg 150 mg 100 mg n/a 150 mg 10 mg 10 mg n/a 20 mg 100 mg n/a 10 mg 10 mg 150 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1008,1009,1010, 1172 2015 2015 2015 1589 Monograph 19 82% CœœHœ÷NœO„ ; Batch 5 is valid until 31 January 2007 96.4% CœŸH–ÕClNOŒŒ ; Batch 3 is valid until 31 August 2006 Batch 2 is valid until 30 June 2006 (1RS)-1-(2,4-dichlorophenyl)-2-(-1H-imidazol-1-yl)ethanol 10000 IU per vial Batch 2 is valid until 31 December 2005 Yes Yes Yes +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a c a a a a a a a a a a a i i a l a a a l a a l a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0080,0081,0093, 0094,1530,1875 1420 1420 1749 1749 1749 1720 1720 20614 0828,1097 1511 0350 0715 0487,0488,0489, 1367 0210,0211,1654 0173 0176 0272,0820 0198,0199 0662,0714,1590 2049 0665,2049 0513,0921,0935, 1017,1018 0665 97.6% EPA ethyl ester 2063,20429 2242 1-(2-ethoxyethyl)-2-(hexahydro-1H-1,4-diazepin-1yl)benzimidaz 2242 ole. 4-(diphenylmethoxy)piperidine 1-[4-(1,1-dimethylethyl)phenyl]-4-(4-hydroxypiperidin-1-yl)butan-1-one Information Unit Sale Quantity Unit 50 mg 1 N,N-dimethyl-2-[1(RS)-1-phenyl-1-(pyridin-4-yl)ethoxy] ethanamine 6 December 2006 1 1 1 2 Erythromycin estolate Erythromycin ethylsuccinate Erythromycin stearate Erythropoietin BRP Esketamine hydrochloride - reference spectrum Esketamine impurity D - * narc Estradiol benzoate Estradiol benzoate impurity E Estradiol butyrate Estradiol hemihydrate Estradiol for peak identification Estradiol valerate E1400000 E1500000 E1500800 E1515000 Y0000324 Y0000338 E1600000 Y0000201 Y0000045 E1620000 Y0000314 Y0000046 © Council of Europe, all rights reserved 2006 4 E1320000 Erythromycin C n/a 1 1 1 1 2 1 1 2 E1310000 Erythromycin B 2 3 2 1 1 4 2 n/a 10 mg 250 mg 10 mg 10 mg 100 mg 10 mg 50 mg 100 mg 100 mg 50 mg 0.25 mg 50 mg 50 mg 50 mg 20 mg 100 mg 0.4 mg 1000 mg 250 mg 250 mg 6 Ergometrine maleate - * Drug Precursor Ergosterol Ergotamine tartrate - * Drug Precursor Erysipelas ELISA coating antigen BRP Erythritol Erythromycin Erythromycin A 500 mg 1 New Y0000712 Eq Influenza Subtype 2 American-like/South Africa Horse Antiserum BRP E0900000 Ergocalciferol E1000000 E1100000 E1200000 Y0000051 Y0000177 E1300000 E1305000 1 mg 2 E0850022 Eq Influenza Subtype 2 European-like/Newmarket Horse Antiserum BRP 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 See leaflet,0249 See leaflet,0249 See leaflet,0249 0210,0211,1654 1512 See leaflet,0249 Monograph 20 estra-1,3,5(10)-triene-3,17alpha-diol 3-benzoate (2R)-2-(2-chlorophenyl)-2-(methylamino)cyclohexanone Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C -20°C +5°C -20°C +5°C -20°C +5°C -20°C -20°C -20°C -20°C -20°C -20°C +5°C -20°C -20°C Leaflet Storage l k a a a a a a a a a b a a i c i c a a a c c c c 79 79 79 79 79 79 79 79 150 79 79 79 79 79 79 79 79 90 79 79 79 79 90 90 90 Extra Price charges 79 a 79 c 90 c 6 December 2006 For extra charges please see 2.2 1742 1742 0139 0139 1614 0821,1203 0821 1614 0082,0574,0575, 0598,1192,1193 0223 0082 0224 0.5ml Freeze dried (0.367g protein) See leaflet,0064 99.8% C÷HŒÕO÷ 1803 960 IU per mg 0179,20702 96.7% C–ŸHÿŸNOŒ– 0179,0274,0293, 0490,0552,1098 99.0% Erythromycin B 0179,0274,0490, 0552,1098 97.6% C–ÿHÿ—NOŒ– ; Batch 3 is valid until 28 February 2006 0179,0274,0490, 0552,1098 0552 0274 0490 32500 IU per vial; 0.250 mg erythropoietin per vial; New unit sale : 1316 only ONE vial 99.8% Cœ‡H÷÷O; Vitamin D2 ; Batch 5 is valid until 28 February 2007 Information Unit Sale Quantity Unit 20 mg 1 86.8% CœœHœ—ClNœO‡ ; Batch 5 is valid until 31 May 2006 15 mg 1 99.7% CŒ‡HœÕOœ 1 mg 3 Assigned SRH antibody titre: 125 mmË +/-20%; Common standard OIE Strain A/eq/Newmarket/77 1 mg 3 Assigned SRH antibody titre: 180 mmË +/- 20%; Common standard OIE Strain A/eq/Newmarket/1/93 1 mg 3 Assigned SRH antibody titre: 155 mmË +/- 20%; Common standard OIE Strain A/eq/Newmarket/2/93 2 6 1 2 Batch E0850021 Eq Influenza Subtype 2 American-like/Newmarket Horse Antiserum BRP Order Reference Standard Code E0600000 4-Epitetracycline hydrochloride Y0000052 Equilin E0850010 Eq Influenza Subtype 1 Strain A/eq/Newmarket/77 Horse Antiserum BRP Catalogue No. 48-2006/4 Ethionamide Ethosuximide Ethosuximide impurity A Ethyl acetate - reference spectrum Ethylcellulose - reference spectrum 1-N-Ethylgaramine sulphate 1,1'-Ethylidenebistryptophan Ethyl indole-3-carboxylate Ethylmorphine hydrochloride - reference spectrum Ethylnicotinamide Ethyl parahydroxybenzoate Etifenin Etilefrine hydrochloride Etilefrine impurity A Etidronate disodium Etodolac Etodolac impurity H Etofenamate Etofenamate for peak identification Etofenamate impurity G Etofylline Etomidate Etomidate impurity B Etoposide Eugenol Famotidine E2000000 E2150000 E2250000 E2195000 E2195900 E2202000 E2205500 Y0000617 E2300000 E2400000 E2425000 E2450000 E2451000 E2451010 Y0000572 E2470000 E2470050 E2499900 E2499901 E2499914 E2500000 E2503000 E2503004 E2600000 E5000000 F0005000 © Council of Europe, all rights reserved 2006 Estriol Estriol impurity A Estrone Etacrynic acid Etamsylate Ethacridine lactate monohydrate Ethambutol hydrochloride Ethanol (anhydrous) - reference spectrum Ethanol 96% - reference spectrum Ethinylestradiol Reference Standard Order Code E1680000 E1680005 E1700000 E1800000 E1830000 E1840000 E1850000 A1202800 E1860100 E1900000 Catalogue No. 48-2006/4 1 1 1 1 1 1 1 1 1 1 1 1 4 2 2 1 1 1 n/a n/a 1 2 1 n/a 1 2 2 1 2 1 1 1 2 n/a n/a 2 Batch 25 mg 75 mg 20 mg 5 mg 60 mg 10 mg 40 mg 15 mg 20 mg 100 mg 100 mg 25 mg 150 mg 500 μl 100 mg 100 mg 30 mg 50 mg n/a n/a 125 mg 5 mg 10 mg n/a 150 mg 50 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Information 21 methyl 1-[(1RS)-1-phenylethyl]-1H-imidazole-5-carboxylate 97.5% Cœ„H–œOŒ– 2-hydroxyethyl 2-[[3-(trifluoromethyl)phenyl]amino]-benzoate 2-(7-ethylindol-3-yl)ethanol 2-ethylamino-1-(3-hydroxyphenyl)ethanone (etilefrone) 88.2% 1-N-Ethylgaramin sulphate 82.3% 1,1'-Ethylidenebistryptophan 2-ethyl-2-methylsuccinic acid Unit Sale Quantity Unit 50 mg 1 20 mg 1 9,11-didehydroestriol 15 mg 1 99.9% CŒ‡HœœOœ 100 mg 1 30 mg 1 50 mg 1 250 mg 1 99.1% CŒÕHœÿClœNœOœ n/a 1 n/a 1 100 mg 1 Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a a a a a a a a a a a l l a a a l a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 l 79 l 79 g For extra charges please see 2.2 1203 1203 1512 0457 1204 1591 0553 1318 1317 0140,0821,0926, 0940 0141 0764 0764 0899 0822 1351 1272,1383 2102 0491 0233 0409,0431,0900, 1262,1263,2134 0585 1205 1205 1778 1422 1422 1513 1513 1513 0492 1514 1514 0823 1100 1012 Monograph 6 December 2006 1 1 1 1 1 1 2 1 1 1 2 3 F0007000 Famotidine impurity B Y0000409 Famotidine impurity D Y0000556 Y0000660 F0030000 Y0000415 F0040000 F0040010 F0040020 F0041000 F0048000 F0048005 1 n/a n/a n/a 1 1 Fenoterol hydrobromide Fenoterol hydrobromide - reference spectrum Fentanyl - reference spectrum Fentanyl citrate - reference spectrum Fenticonazole nitrate Fenticonazole impurity D Ferrous gluconate Finasteride Finasteride for system suitability Flecainide acetate Flecainide impurity A Flecainide impurity B Flubendazole Flubendazole for system suitability Flucloxacillin sodium F0050000 F0051000 F0054990 F0055000 F0060000 F0060040 F0100000 Y0000090 Y0000091 F0120000 F0120005 F0120010 Y0000138 Y0000139 F0150000 © Council of Europe, all rights reserved 2006 3 F0048035 Fenofibrate impurity G 1 1 1 6 1 1 1 1 1 3 F0048010 Fenofibrate impurity B Febantel Febantel for system suitability Felodipine Felypressin Fenbendazole Fenbendazole impurity A Fenbendazole impurity B Fenbufen Fenofibrate Fenofibrate impurity A 1 1 Batch Order Reference Standard Code Y0000382 Famotidine for system suitability F0006000 Famotidine impurity A Catalogue No. 48-2006/4 25 mg 25 mg 20 mg 250 mg 1000 mg 50 mg 100 mg 200 mg 50 mg 100 mg n/a n/a n/a 50 mg 20 mg 25 mg 10 mg 10 mg 120 mg 0.994 mg 150 mg 20 mg 20 mg 100 mg 100 mg 20 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0901 0901 1210 1103 1211 1211 1322 1322 2176 2176 1013 1634 1208,1458 1208 1208 1209 1322 1322 1012 1012 1012 1012 Monograph 22 95.3% CŒ„HŒÿClFN–NaO—S ; Batch 5 is valid until 30 April 2006 Yes Yes Yes Yes +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a c a a a a a a l l l a a a a a a a c a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 1721 1721 0661,0663,0668 0493 1615 1615 1324 3-[2,5-bis(2,2,2-trifluoroethoxy)phenyl]-1,5,6,7,8,8a-hexahydro 1324 imidazo[1,5-a]pyridine (piperidin-2-yl)methanamine 1324 99.8% Cœ–H–ÿNœOœ (¢£)-1-[2-(2,4-dichlorophenyl)-2-hydroxyethyl]-3-[4-(phenyl suphanyl)benzyl]imidazolium nitrate 100.0% CœÕHœŒClO÷ (4-chlorophenyl)(4-hydroxyphenyl)methanone ; Batch 2 is valid until 31 May 2006 2[4-(4-chlorobenzoyl)phenoxy]-2-methylpropanoic acid (fenofibric acid) 1-methylethyl 2-[[2-[4-(4-chlorobenzoyl)phenoxy]-2-methyl propanoyl] oxy]-2-methylpropanoate contains 4.0% m/m of the diastereoisomers methyl(1§-benzimidazol-2-yl)carbamate methyl[5(6)-chlorobenzimidazol-2-yl]carbamate Information Unit Sale Quantity Unit 10 mg 1 10 mg 1 3-[[[2-[(diaminomethylene)amino]thiazol-4-yl]methyl]-thio] propanamide 10 mg 1 3,5-bis[2-[[[2-[(diaminomethylene)amino]thiazol-4-yl]methyl] thio]-ethyl]-4§-1,2,4,6-thiatriazine1,1-dioxide 10 mg 1 3-[[[2-[(diaminomethylene)amino]thiazol-4-yl]methyl]sulphanyl] propanamide 110 mg 1 99.9% CœÕHœœN÷OÿS 6 December 2006 1 3 n/a 1 1 n/a 1 1 1 3 1 1 n/a 1 3 4 3 1 2 1 Y0000078 Flupentixol impurity F F0260000 Fluphenazine decanoate Y0000009 Fluphenazine enantate © Council of Europe, all rights reserved 2006 1 1 Y0000064 Flupentixol dihydrochloride Y0000067 Flupentixol impurity D Flumetasone pivalate Flunarizine dihydrochloride Flunarizine dihydrochloride - reference spectrum Flunarizine dihydrochloride for system suitability Flunitrazepam - * psy Flunitrazepam - reference spectrum Flunixin meglumine Flunixin impurity B Flunixin impurity C Fluocinolone acetonide Fluocortolone pivalate Diacetylfluorescein Fluoresceine sodium - reference spectrum Fluorouracil Fluoxetine hydrochloride Fluoxetine impurity B (methyl(3-phenylpropyl)amine) Fluoxetine impurity C F0188500 F0189900 Y0000265 Y0000266 F0190000 Y0000169 Y0000443 Y0000444 Y0000445 F0200000 F0230000 Y0000454 F0245000 F0250000 F0253000 F0253020 F0253030 1 1 1 1 1 1 2 n/a 1 Batch 1 2 Fluconazole Fluconazole for peak identification Fluconazole impurity B Fluconazole impurity C Flucytosine Fludarabine phosphate Fludrocortisone acetate Flumazenil - reference spectrum Flumazenil impurity B Reference Standard F0189000 Flumequine F0189020 Flumequine impurity B Order Code Y0000557 Y0000558 Y0000573 Y0000574 F0175000 Y0000419 New F0180000 F0188000 Y0000335 Catalogue No. 48-2006/4 60 mg 100 mg 25 mg 120 mg 15 mg 100 mg 100 mg n/a 20 mg 100 mg n/a 10 mg 10 mg 50 mg 100 mg 100 mg 100 mg n/a 50 mg 250 mg 5 mg 5 mg 60 mg 0.1 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2287 2287 2287 2287 0766 1781 0767 1326 1326 Monograph 23 2-[2-[4-[3-[(EZ)-2-(trifluoromethyl)-9H-thioxanthen-9ylidene]propyl]piperazin-1-yl]ethoxy]ethanol 2-[4-[(EZ)-3-[(9RS)-2-(trifluoromethyl)-9H-thioxanthen-9-yl] prop-2-enyl]piperazin-1-yl]ethanol methyl(3-phenylpropyl)amine (¢£)-methyl-[3-phenyl-3-(3-trifluoromethylphenoxy)-propyl] amine ; Batch 2 is valid until 31 January 2006 99.6% Cœ÷HŒÿOŸ 2-methyl-3-(trifluoromethyl)aniline ethyl 2-chloropyridine-3-carboxylate 100% Cœ÷H–ÕFœOÿ. Dried at 100-105°C for 2 hours Batch 2 is valid until 31 October 2006 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a l a j l a a a a a a l a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 l 79 a For extra charges please see 2.2 1014,1015 1014,1015 1693 1693 1693 1327 0816 1722 1722 1280 0717 1696 1696 1696 0494 1212 1213 1213 0611,0766 1104 1104 1104 1517 ethyl(RS)-9-fluoro-5-methyl-1-oxo-6,7-dihydro-1H,5H-benzo[i,j] 1517 quinolizine-2-carboxylate (flumequine ethyl ester) ; Batch 1 is valid until 30 June 2006 Information Unit Sale Quantity Unit 50 mg 1 10 mg 1 10 mg 1 94.6% CŒ—HŒ÷N„OF 5 mg 1 100 mg 1 100 mg 1 97.6% CŒÕHŒ–FN—OŸP 100 mg 1 Batch 1 is valid until 30 April 2007 n/a 1 5 mg 1 8-fluoro-5-methyl-6-oxo-5,6-dihydro-4H-imidazo[1,5-a][1,4] benzodiazepine-3-carboxylic acid 6 December 2006 2 1 3 F0600000 Fumaric acid F0700000 Furosemide F0702000 Furosemide impurity A © Council of Europe, all rights reserved 2006 1 1 1 1 7 2 1 1 2 1 1 n/a n/a 1 1 F0550000 Fructose Flutrimazole Flutrimazole impurity B Foeniculin for peak identification Folic acid Formoterol fumarate dihydrate Formoterol fumarate dihydrate for impurity I identification Formoterol fumarate for system suitability Formylfolic acid Foscarnet sodium hexahydrate Foscarnet impurity B Fosfomycin calcium - reference spectrum Fosfomycin sodium - reference spectrum Fosfomycin trometamol Fosfomycin trometamol impurity A F0290000 F0290010 Y0000386 F0300000 F0372000 Y0000339 Y0000340 F0380000 F0389000 F0389004 F0399900 F0399950 F0400000 F0400010 1 1 1 1 3 Flutamide Flutamide impurity C Fluticasone propionate Fluticasone impurity D F0285600 F0285603 Y0000284 Y0000221 1 1 1 n/a 1 1 1 1 Batch F0450000 Framycetin sulphate Fluphenazine dihydrochloride Fluphenazine octanoate Fluphenazine sulphoxide Flurazepam monohydrochloride - reference spectrum Flurbiprofen Flurbiprofen impurity A Fluspirilene Fluspirilene impurity C Reference Standard Order Code F0280000 Y0000298 Y0000299 Y0000211 F0285200 F0285202 Y0000236 Y0000375 Catalogue No. 48-2006/4 100 mg 5 mg 100 mg 100 mg 25 mg 100 mg 60 mg 100 mg 250 mg 10 mg 10 mg 10 mg 30 mg 50 mg 10 mg n/a n/a 1500 mg 50 mg 50 mg 20 mg 100 mg 10 mg 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 24 2-chloro-4-(furfurylamino)-5-sulphamoylbenzoic acid 99.6% CŸHŒ‡NOŸP 1,3-dihydroxy-2-(hydroxymethyl)propan-2-aminium (1,2-dihydroxypropyl)phosphonate 18060 IU per vial, 95.2% Cœ–H÷ÿNÿOŒ–,xHœSO÷ disodium (ethoxyoxydophosphanyl)formate 10-Formylfolic acid (RS)-(2-fluorophenyl)(4-fluorophenyl)phenylmethanol Star anise oil 91.5 % CŒ„HŒ„NŸOÿ Batch 1 is valid until 30 November 2006 N-[4-nitro-3-(trifluoromethyl)phenyl]propanamide 99.1% Cœ—H–ŒF–O—S S-methyl 6a,9a-difluoro-11b-hydroxy-16a-methyl-3-oxo-17apropionyloxy-androsta-1,4-diene-17ß-carbothioate (S-methyl derivative) Information Unit Sale Quantity Unit 50 mg 1 10 mg 1 10 mg 1 n/a 1 50 mg 1 20 mg 1 (2RS)-2-(biphenyl-4-yl)propanoic acid 20 mg 1 10 mg 1 8-[4,4-bis(4-fluorophenyl)butyl]-3-(hydroxymethyl)-1-phenyl -1,3,8-triazaspiro[4.5]decan-4-one Yes Yes Yes +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a a a a a c a a l l a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 l 79 a 79 a 79 a 79 a For extra charges please see 2.2 0177,0178,0187, 0188,0204,0209, 1061,1570 0365,0902,1190, 1592 0391 0391 0180,0197,20702 1424 1424 0804 0067 1293,1724 1724 1724 0978,1606 1520 1520 1328 1329 1425 1425 1423 1423 1750 1750 0904,1014 1014,1015 1014,1015 0905 1519 1519 1723 1723 Monograph 6 December 2006 1 1 1 1 Y0000515 Y0000516 G0340000 G0342000 1 1 1 1 1 1 n/a 1 2 Y0000643 Glipizide impurity D Y0000191 Human glucagon G0350500 Glucose G0355000 Glutamic acid Y0000517 G0360000 G0400000 G0400002 G0400004 © Council of Europe, all rights reserved 2006 Glutathione Glutethimide - * psy Glycerol (85 per cent) - reference spectrum Glycerol dibehenate Glycerol distearate 1 Y0000523 Glipizide impurity C Glimepiride Glimepiride for system suitability Glipizide Glipizide impurity A 2 2 2 G0326000 Gliclazide G0326004 Gliclazide impurity B G0326012 Gliclazide impurity F n/a 1 2 1 1 1 1 1 1 5 2 2 1 Batch 1 Fusidic acid - reference spectrum Galactitol Galactose Gallamine triethiodide Gammacyclodextrin Gemcitabine hydrochloride Gemcitabine impurity A Gemfibrozil Gemfibrozil for system suitability Gentamicin sulphate Gitoxin Glibenclamide Glibenclamide impurity A Reference Standard Y0000242 Glibenclamide impurity B Order Code F1000000 G0049000 G0050000 G0100000 G0150000 Y0000675 Y0000676 Y0000513 Y0000514 New G0200000 G0300000 G0325000 G0325010 Catalogue No. 48-2006/4 10 mg 50 mg n/a 2000 mg 2000 mg 50 mg 10 mg 0.952 mg 100 mg 10 mg 0.012 mg 50 mg 10 mg 1 1 1 1 1 1 1 2 1 1 1 1 1 25 0.952 mg pure human glucagon per vial 4-[2-(5-methylpyrazine-2-carboxamido)ethyl]benzene sulphonamide ethyl [2-[4-[(cyclohexylcarbamoyl)sulphamoyl]phenyl]ethyl] carbamate Information Unit Sale Quantity Unit n/a 1 50 mg 1 60 mg 1 Batch 1 is valid until 31 August 2006 100 mg 1 50 mg 1 50 mg 1 99.9% C„HŒœClFœN–O÷ 20 mg 1 5 mg 1 0.196 mg 1 25 mg 2 16500 IU per vial ; Batch 4 is valid until 31 March 2007 30 mg 1 100 mg 1 100 mg 1 4-[2-(5-chloro-2-methoxybenzamido)ethyl]benzenesulphonamide 10 mg 1 methyl [[4-[2-[(5-chloro-2-methoxybenzoyl)amino]ethyl]phenyl] sulphonyl]carbamate 20 mg 1 Batch 1 is valid until 31 August 2006 25 mg 1 2-nitroso-octahydrocyclopenta[c]pyrrole 25 mg 1 1-(hexahydrocyclopenta[c]pyrrol-2(1H)-yl)-3-[(2-methylphenyl) sulphonyl]urea 60 mg 1 99.4% Cœ÷H–÷N÷O—S Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C Leaflet Storage a j l a a a a c a a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 l 79 a 79 a 79 a 79 a 79 g 79 g 79 a 79 a 79 c 79 a 79 a 79 a For extra charges please see 2.2 0906 1635 0177,0178,0187, 0188,0204,0209, 1061,1215,1570 0750,0797,1445, 2076 1670 1291 0496,0497 1427 1428 0906 2223 2223 0906 0906 0718,1524 1524 1524 0718 0798,0848 1381 1215 0181 1070,1487 2306 2306 1694 1694 0331,20702 0078,0079,2168 0718 0718 Monograph 6 December 2006 Glycerol monolinoleate Glycerol mono-oleate Glycerol monostearate 40-55 Glyceryl trinitrate - reference spectrum Glyceryl trinitrate solution Glycine Ammonium glycyrrhizate Glycyrrhizate (monoammonium) Gonadorelin Goserelin Gosereline - reference spectrum 4-D-Ser-goserelin Goserelin validation mixture Gramicidin Granisetron hydrochloride Granisetron impurity A Reference Standard 2 2 1 2 © Council of Europe, all rights reserved 2006 Hepatitis B vaccine (rDNA) BRP method A (thiomersal free) Hepatitis B vaccine (rDNA) BRP method B Hepatitis C Virus RNA for NAT testing BRP Heptadecanol Y0000389 H0210010 H0215000 H0220000 1 n/a 4 1 3 1 2 1 1 1 1 1 2 Haloperidol decanoate Halothane - reference spectrum Heparin Low-Molecular-Mass for assay BRP Heparin Low-Molecular-Mass for calibration CRS Heparin sodium BRP Granisetron impurity E Griseofulvin Guaiacol Guaifenesin Halofantrine hydrochloride Halofantrine impurity C Haloperidol 1 1 1 2 n/a 2 3 1 1 4 1 n/a 1 1 1 1 1 Batch H0205010 Hepatitis A vaccine (inactivated, adsorbed) Type B BRP H0100100 H0150000 H0185000 H0190000 H0200000 Y0000395 G0600000 New Y0000619 G0700000 Y0000117 Y0000118 H0100000 Y0000478 Granisetron impurity B Order Code G0400006 G0400007 G0400008 G0400101 G0400100 New G0450000 Y0000433 G0460000 G0525000 Y0000125 Y0000126 Y0000019 Y0000194 G0550000 Y0000396 Y0000477 Catalogue No. 48-2006/4 0.5 ml 1 ml 40 mg 600 mg 0.5 ml 60 mg n/a 1 ml 25 mg 2 ml 100 mg 125 mg 10 mg 50 mg 2 2 5 1 3 1 1 5 1 1 1 1 1 1 1695 0182 1978 0615 1979 1979 0616,0995,1178, 1503 1397,1431 0393 See leaflet,0828 0828 0332,0333,0569, 0686,20705 See leaflet,20714 1695 1429 1430 0495 1331 1331,1355 0614,0752 1772 0277,1536,1772 0827 1636 1636 1636 1636 0907,1662,20702 1695 1695 Monograph 26 Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C Leaflet Storage b b e a b a l b a a a a a a a a a a 79 242 90 90 90 79 90 90 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 l 79 g 79 a 79 a 79 a 79 c 79 c 79 l 79 c 79 c 79 a 79 a 79 a For extra charges please see 2.2 262 IU per ml; Please contact us for information on the type needed for your use 16.6 micrograms per ml See leaflet,20715 20 micrograms per ml See leaflet,1056 HCV-RNA content 500 IU per vial; For plasma pool testing by NAT See leaflet,20621 0801,0802,0847 Anti-IIa activity : 33 IU per ml; Anti-Xa activity : 113 IU per ml. Mn = 3700 1010 IU per ml ; Batch 2 is valid until 31 January 2007 99.6% CœÿH–ŒCl–F–NO [1,3-dichloro-6-(trifluoromethyl)phenantren-9-yl]methanol Information Unit Sale Quantity Unit 2000 mg 1 2000 mg 1 2000 mg 1 Batch 1 is valid until 30 September 2006 n/a 1 0.5 ml 1 1% m/m in ethanol ; Batch 1 is valid until 28 February 2007 50 mg 1 Batch 2 is valid until 28 February 2007 70 mg 1 300 mg 1 80.6% C÷œHÿ—NOŒÿ 5.08 mg 1 5.08 mg per vial of C——HŸ—NŒŸOŒ– 4.93 mg 1 4.93 mg per vial of C—„H‡÷NŒ‡OŒ÷ n/a 1 0.1 mg 1 1 mg 1 Supplied with the Ph. Eur. reference chromatogram 250 mg 1 1081 IU per mg 120 mg 1 99.8% CŒ‡Hœ—ClN÷O 1 mg 1 2-methyl-N-[(1R,3r,5S)-9-methyl-9-azabicyclo[3.3.1]non-3-yl]-2 H-indazole-3-carboxamide 1 mg 1 N-[(1R,3r,5S)-9-methyl-9-azabicyclo[3.3.1]non-3-yl]-1H-indazole -3-carboxamide 10 mg 1 endo-3-amino-9-methyl-9-azabicyclo[3.3.1]nonane 50 mg 1 Batch 1 is valid until 30 June 2006 2200 mg 1 99.5% CŸH‡Oœ 6 December 2006 1 1 3 1 1 © Council of Europe, all rights reserved 2006 1 1 1 1 1 1 4 1 1 1 Y0000488 Human immunoglobulin (molecular size) BRP Human Plasma Pools for NAT validation Human rabies immunoglobulin BRP Human tetanus immunoglobulin BRP Human vaccinia immunoglobulin Hyaluronidase BRP Hydralazine hydrochloride Hydrochlorothiazide Hydrocodone hydrogen tartrate 2.5-hydrate - * narc Hydrocodone for peak identification - * narc 2 H1000000 Human immunoglobulin for electrophoresis BRP H1005000 H1100000 H1110000 Y0000502 H1115000 H1120000 H1200000 New Y0000646 New Y0000710 2 H0990000 Human immunoglobulin BRP Human anti-D immunoglobulin BRP Human coagulation factor VII concentrate BRP Human coagulation factor VIII concentrate BRP Human coagulation factor IX concentrate BRP Human hepatitis A immunoglobulin BRP Y0000219 Y0000667 H0920000 H0920500 H0950000 1 1 3 1 1 1 1 4 1 2 1 1 1 1 n/a Batch 1 Reference Standard Heptaminol hydrochloride Heptaminol impurity A alpha-Hexachlorocyclohexane Hexamidine diisetionate Hexetidine Hexobarbital Hexylresorcinol Hide powder Histamine dihydrochloride Histamine phosphate Histidine Histidine hydrochloride monohydrate Homatropine hydrobromide Homatropine methylbromide L-Homocysteine thiolactone hydrochloride - reference spectrum H0900000 Human albumin for electrophoresis BRP Order Code Y0000063 Y0000057 H0250000 H0330000 H0325000 H0400000 H0420000 H0500000 H0600000 H0700000 H0750000 H0755000 H0800000 H0830000 H0837000 Catalogue No. 48-2006/4 3502 mg 170 mg 87 mg 1 ml 50 mg 20 mg 150 mg 10 mg 10 mg 700 mg 96 mg 1320 mg 1 uc 26 mg 34 mg 30 mg 10 mg 1000 mg 1 3 1 3 1 1 1 1 1 3 1 3 1 2 5 5 3 1 27 Batch 3 is valid until 30 November 2006 Set of 103 plasma pool samples 91 IU per vial 120 IU per vial 23 IU per vial 328 IU per mg 75.7% to 80.9% of the total protein is the main band (Ig), protein content: 5% Each vial contains 0.7 gram of immunoglobulin G Contains 1.0 mg Immunoglobulin G per vial 96,7% to 98,7% of the total protein is the main band (albumin), protein content : 5% 285 IU anti-D immunoglobulin per ampoule 8.2 IU per vial 8.6 IU per vial; Common standard with FDA Common standard with FDA 10.2 IU per vial Information Unit Sale Quantity Unit 150 mg 1 30 mg 1 (2RS)-6-methylhept-5-en-2-amine 10 mg 1 50 mg 1 100 mg 1 500 mg 1 100 mg 1 500 mg 1 250 mg 1 250 mg 1 100 mg 1 100 mg 1 100 mg 1 25 mg 1 n/a 1 Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes Yes -20°C -20°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C -20°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c c c b a a a k k a a a c c c c c a 79 79 79 79 79 270 90 90 400 90 79 90 90 90 90 79 90 79 Extra Price charges 79 a 79 a 79 a 79 g 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 l For extra charges please see 2.2 See leaflet, 0338, 0918,1928 See leaflet,20621 See leaflet,0723 0398 See leaflet 0912 0829 0394,0546 1784 1784 See leaflet,20713 See leaflet,20710 See leaflet,20704 See leaflet,20711 See leaflet,0338, 0769 See leaflet,0338, 0918 0338,0918 0255 1980 1980 0772 1436 1221 0183 1437 20814 0143 0144 0911 0910 0500,0720 0720 1617 Monograph 6 December 2006 1 1 n/a 3 2 1 1 1 n/a H1600000 Hyoscyamine sulphate Y0000449 Hyoscyamine impurity E H5000000 Hypromellose phthalate - reference spectrum I0020000 Ibuprofen B1220000 Ibuprofen impurity B Y0000140 I0050000 I0060000 I0060100 © Council of Europe, all rights reserved 2006 Ibuprofen impurity F Idoxuridine Ifosfamide Ifosfamide - reference spectrum 1 1 H1500000 Hyoscine hydrobromide Y0000448 Hyoscine hydrobromide impurity B 2 1 1 n/a 1 1 1 2 1 1 2 1 1 1 1 1 1 1 Hydrocortisone hydrogen succinate Hydrogenated wool fat Hydromorphone hydrochloride - * narc Hydrous benzoyl peroxide - reference spectrum Hydroxocobalamin Hydroxycarbamide Hydroxyethyl salicylate 4-Hydroxyphenoxymethylpenicillin D-alpha-(4-Hydroxy-phenyl)glycine Hydroxypropylbetadex Hydroxyzine hydrochloride Hymecromone Hymecromone impurity A Hymecromone impurity B Hyoscine Hyoscine impurity A 8 7 Batch H1450000 Hyoscine butylbromide Y0000447 Hyoscine butylbromide impurity E H1425000 H1426000 Y0000446 B0650000 H1428000 Y0000119 H1429400 H1429700 H1430000 Y0000186 H1435000 Y0000011 Y0000012 Y0000013 Y0000483 Y0000484 Order Reference Standard Code New H1300000 Hydrocortisone H1400000 Hydrocortisone acetate Catalogue No. 48-2006/4 5 mg 50 mg 50 mg n/a n/a 100 mg 1.15 ml 100 mg 10 mg 50 mg 10 mg 25 mg 10 mg 100 mg 250 mg 10 mg n/a 10 mg 175 mg 125 mg 50 mg 50 mg 10 mg 600 mg 100 mg 25 mg 25 mg 10 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 28 100.0% CŸHŒ—ClœNœOœP solution of 0.06% m/V in acetonitrile (2RS)-2-(4-Butylphenyl)propanoic acid - to be diluted as appropriate. 3-[4-(2-methylpropyl)phenyl]propanoic acid (1R,3r,5S)-8-azabicyclo[3.2.1]oct-3-yl(2S)-3-hydroxy-2-phenyl -propanoate (1R,2R,4S,5S,7s)-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate (1R,2R,4S,5S,7S)-9-butyl -7-[[(2S)-3-hydroxy2-phenylpropanoyl]oxy]-3-oxa -9-azoni atricyclo [3.3.1.02,4]nonane (1R,2R,4S,5S,7s)-3-oxa-9-azatricyclo[3.3.1.02,4]non-7-yl (2S)-3-hydroxy-2-phenylpropanoate (norhyoscine) Resorcinol 7-hydroxy-2-methyl-4H-1-benzopyran-4-one. 98.8% CŒÿHŒ‡NœOÿ 99.9% CH÷NœOœ Batch 1 is valid until 31 December 2005 Information Unit Sale Quantity Unit 100 mg 1 Batch 7 is valid until 31 March 2007 125 mg 1 0721 0669 1529 1529 0347 0721 0721 0501 0501 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C Leaflet Storage a a a l l a g g g g g a a a a k l a a a a a a a a a a g g 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 0106,0500 0106 0737 0737 0335,0353,0561 0321,0334,0734, 0767 0768,1131 0969 2099 0704 0913,0914,0915 1616 1225 0148,0149 0813 1804 0916,1086,1092 1786 1786 1786 2167 2167 Monograph 6 December 2006 1 3 2 3 1 2 1 1 1 1 1 1 1 1 1 1 Insulin (bovine) Insulin (human) Iohexol impurity J I0310000 Y0000348 Insulin lispro I0320000 Insulin (porcine) Interferon alfa-2a Interferon alfa-2b Interferon gamma 1b Interferon gamma-1b validation solution Iobenguane sulphate Iohexol Iohexol impurity A I0305000 I0320300 I0320301 I0320330 I0320331 I0328000 I0320800 I0320810 I0320820 Y0000672 Iohexol for peak identification I0329000 Iopamidol I0329010 Iopamidol impurity A Y0000406 Iopamidol impurity H I0330000 I0340000 © Council of Europe, all rights reserved 2006 Iopanoic acid Iotalamic acid 3 Immunoglobulin panel for anti-D antibodies test BRP Indapamide Indapamide impurity B Indometacin Insulin aspart 3 1 3 2 1 1 1 1 1 1 1 1 2 Y0000540 I0150000 I0150020 I0200000 Y0000349 Batch Ifosfamide impurity A Ifosfamide impurity B Ifosfamide impurity E Ifosfamide impurity F Imidazole Imipenem Imipramine hydrochloride Reference Standard Order Code I0060002 I0060004 I0060010 I0060012 I0086000 I0090000 I0100000 Catalogue No. 48-2006/4 100 mg 100 mg 10 mg 10 mg 50 mg 10 mg 125 mg 1 ml 0.2 ml 0.6 ml 0.2 ml 50 mg 150 mg 50 mg 5.93 mg 8.61 mg 7.03 mg 7.99 mg 2000 mg 150 mg 5 mg 50 mg 3.89 mg 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 29 0700 0751 Yes Yes Yes Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C -80°C -80°C -80°C -80°C +5°C +5°C +5°C -20°C -20°C -20°C -20°C -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C Leaflet Storage a a a a a a a d d d d a a a c c c c a a a g c 79 79 79 79 79 79 79 79 79 79 79 90 90 90 90 90 90 90 90 79 79 79 90 Extra Price charges 79 a 79 a 79 a 79 b 79 a 79 c 79 g For extra charges please see 2.2 1114 1115 1115, 1754 1114 0838,0854,1637, 1638 2085 0838,0854,1637, 1638 1110 1110 1440 1440 1111,1112,1113 1114 1114 0854,1637 1529 1529 1529 1529 1424 1226 0029,0408,0817, 0889,1787 See leaflet, 20626 1108 1108 0092,0922 2084 Monograph N,N'-bis[2-hydroxy-1-(hydroxymethyl)ethyl]-5-amino-2,4,6-triiodoisophthalamide 4-chloro-N,N'-bis(2-hydroxy-1-(hydroxymethyl)ethyl)-5-(2-hydro 1115 xypropanoyl)amino)2,6-diiodobenzenz-1,3-dicarboxamide 5-acetamido-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-tri-iodo benzene-1,3-dicarboxamide 5-amino-N,N'-bis(2,3-dihydroxypropyl)-2,4,6-tri-iodobenzene-1, 3-dicarboxamide About 1.46 mg per ml about 7.19 mg per ml about 1 mg per ml about 1 mg per ml 3.89 mg [insulin aspart + B28isoAsp insulin aspart + A21Asp insulin aspart + B3Asp insulin aspart + B3isoAsp insulin aspart] per vial 7.99 mg insulin + A21 desamido per vial ; Batch 2 is valid until 28 February 2006 7.03 mg insulin + A21 desamido per vial ; Batch 2 is valid until 31 March 2006 5.93 mg insulin lispro per vial 8.61 mg [porcine insulin + A21-desamido porcine insulin] per vial 97.7% CŒÿHŒÿClN–O–S 4-chloro-3-sulphamoyl-N-(2-methyl-1H-indol-1-yl)-benzamide Information Unit Sale Quantity Unit 30 mg 1 3-[(2-chloroethyl)amino]propyl dihydrogen phosphate 20 mg 1 bis[3-[(2-chloroethyl)amino]propyl] dihydrogen diphosphate 10 mg 1 3-chloro-N-(2-chloroethyl)propan-1-amine 10 mg 1 (RS)-2-chloro-3-(2-chloroethyl)-1,3,2-oxazaphosphinane 2-oxide 100 mg 1 100 mg 1 92.8% CŒœHŒŸN–O÷S 50 mg 1 Batch 1 is valid until 30 June 2006 6 December 2006 1 1 2 Itraconazole Ivermectin I7000000 I8000010 Y0000041 Josamycin Y0000042 Josamycin propionate K0100000 Kanamycin B sulphate © Council of Europe, all rights reserved 2006 2 1 Isoconazole Isoconazole nitrate Isoemetine hydrobromide Isoflurane - reference spectrum Isoleucine Isomalt Isomaltooligosaccharide Isoniazid Isoprenaline hydrochloride Isoprenaline sulphate Isopromethazine hydrochloride Isopropyl hexadecanoate Isopropyl tetradecanoate Isosorbide dinitrate Isosorbide mononitrate Isosorbide-2-nitrate Isotretinoin Isoxsuprine hydrochloride Isradipine Isradipine impurity D I0375000 I0380000 I0400000 Y0000037 I0460000 I0465000 Y0000070 I0500000 I0599990 I0600000 I0700000 I0725000 I0750000 I0775000 I0775010 I0775020 I0800000 I0900000 Y0000366 Y0000367 1 1 1 n/a 1 2 1 1 1 2 4 2 3 1 2 2 3 1 1 1 3 Ipratropium bromide impurity B I0361000 1 1 1 1 Batch 5 1 Iotrolan Iotrolan for system suitability Ioxaglic acid Ioxaglic acid impurity A Reference Standard I0360000 Ipratropium bromide Y0000276 Ipratropium bromide impurity A Order Code Y0000555 New Y0000658 Y0000141 Y0000142 Catalogue No. 48-2006/4 150 mg 150 mg 20 mg 150 mg 150 mg 200 mg 200 mg 25 mg n/a 50 mg 3000 mg 0.9 mg 100 mg 50 mg 500 mg 50 mg 100 mg 2 ml 250 mg 100 mg 50 mg 60 mg 50 mg 125 mg 5 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 30 99.2% CŒ„HœŒN–O— methyl 1-methylethyl 4-(2,1,3-benzoxadiazol-4-yl) -2,6-dimethylpyridine-3,5-dicarboxylate Batch 1 is valid until 31 January 2007 83.9% C÷‡HŸ÷OŒ÷ (compound HœBŒ´); 5.9% C÷ŸHŸœOŒ÷ (compound HœBŒÇ) 1000 Ph. Eur. units per mg 930 Ph. Eur. units per mg Batch 1 is valid until 31 December 2006 Batch 3 is valid until 31 August 2006 94.3% CŒ„H–‡Oœ 98.8% CŒŸH–÷Oœ 24.5% CÿH‡NœO‡ 99.9% CÿH„NOÿ; Isosorbide-5-nitrate 96.6% CŒœHœ÷OŒŒ ; Batch 1 is valid until 31 July 2006 Information Unit Sale Quantity Unit 100 mg 1 5 mg 1 125 mg 1 20 mg 1 3-amino-5[[(2-hydroxyethyl)amino]carbonyl]-2,4,6-trioiodobenzoic acid 120 mg 1 Batch 4 is valid until 31 October 2006 5 mg 1 (1R,3r,5S,8r)-3-hydroxy-8-methyl-8-(1-methylethyl)-8-azoniabicyclo[3.2.1]octane 10 mg 1 (1R,3r,5S,8s)-3-[[(2RS)-3-hydroxy-2-phenylpropanoyl]oxy]-8methyl-8-(1-methylethyl)-8-azoniabicyclo[3.2.1]octane Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a l a a a a a a a a a g h f a a g g a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a For extra charges please see 2.2 1982,1983,20702 1982,1983,20702 0032,0033,0645 1335 1336 1018 1017 0080,0081 1673 0770 1531 1506 0146 1332 0502 0524 0839 0725 1117,1118 1117,1118 1117,1118 0693,1019 1119 2110 2110 0919 0919 0772 1754 1754 2009 2009 Monograph 6 December 2006 Labetalol hydrochloride Lactitol monohydrate Lactobionic acid Lactose (anhydrous) Lactose L0050000 L0129000 Y0000257 A1206000 L0100000 © Council of Europe, all rights reserved 2006 L0376001 Leuprorelin - reference spectrum Lactulose Lactulose for system suitability Lamivudine Lamivudine for system suitability 1 Lamivudine for system suitability 2 Leflunomide Letrozole Leflunomide impurity A Leflunomide for peak identification Leucine Leuprorelin 3-Ketofusidic acid Ketoprofen Ketoprofen impurity A Ketoprofen impurity C Ketorolac trometamol Ketorolac trometamol for peak identification Ketotifen hydrogen fumarate - reference spectrum Ketotifen impurity G K1000000 K2000000 K2000010 K2000015 Y0000486 Y0000626 Y0000164 Y0000161 L0130000 Y0000188 Y0000425 Y0000518 Y0000426 New Y0000654 Y0000685 New Y0000487 New Y0000674 L0375000 L0376000 1 1 n/a 1 1 1 Ketamine hydrochloride - * narc Ketamine impurity A Ketobemidone hydrochloride - reference spectrum Ketobemidone impurity B Ketobemidone impurity C Ketoconazole Y0000450 K0551000 Y0000246 Y0000244 Y0000245 K0600000 n/a 2 2 1 1 1 1 1 1 1 2 4 1 2 1 1 1 3 2 3 2 1 1 n/a 2 2 Batch Order Reference Standard Code K0200000 Kanamycin monosulphate Catalogue No. 48-2006/4 n/a 3000 mg 12 mg 150 mg 10 mg 10.3 mg 100 mg 70 mg 25 mg 1 mg 50 mg 0.925 mg 80 mg 60 mg 100 mg 100 mg 100 mg 10 mg 50 mg 5 mg 5 mg 10 mg 5 mg n/a 3 mg 10 mg 50 mg n/a 5 mg 5 mg 150 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Information Monograph 31 1442 Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage l a a a a a g a g g a c a a a a a a g a a g g l a k a l a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0923 93.8% CŒœHœ÷OŒŒ 1337 1647 1061 0177,0178,0187, 0188,0204,0209, 1215,1570 99.7% CŒœHœœOŒŒ 0924,1230 0924,1230 99.7% C‡HŒŒN–O–S 2217 2217 2217 2330 99.7% CŒŸHŒŒN— 2334 4-(trifluoromethyl)aniline 2330 2330 0771,0874 0.925 mg per vial of pure leuprorelin peptide C—„H‡÷NŒÿOŒœ ; Batch 1442 3 is valid until 31 July 2006 0032,0033,0053, 0485,0645,1289, 1290,20702 1020 1-[(2-chlorophenyl)(methylimino)methyl]cyclopentanol 1020,1742 1746 1-(4-(3-hydroxyphenyl)-1-methyl-4-piperidyl)ethanone 1746 1-(4-(3-hydroxyphenyl)-4-piperidyl)propan-1-one 1746 0921,1067,1270, 1335 Batch 2 is valid until 30 September 2006 0798,0848 Batch 1 is valid until 30 September 2006 0922,1157,1209 3-acetylbenzophenone 0922 2-(3-carboxyphenyl)propionic acid 0922 1755 1755 1592 4-(1-methylpiperidin-4-ylidene)-4H-benzo(4,5)cyclohepta(1,2-b) 1592 thiophen-9,10-dione Unit Sale Quantity Unit 150 mg 1 799 IU per mg 6 December 2006 Lithocholic acid Lobeline hydrochloride Lomustine Loperamide hydrochloride Loperamide hydrochloride for system suitability Loperamide oxide monohydrate Loratadine Loratadine for system suitability Loratadine impurity F Loratadine impurity H Lorazepam - * psy Lorazepam for system suitability Lorazepam impurity D Levomepromazine hydrochloride Levomepromazine maleate Levonorgestrel Levothyroxine sodium Lidocaine Lidocaine hydrochloride Lincomycin hydrochloride Lindane Liothyronine sodium Lisinopril dihydrate Lisinopril dihydrate for performance test Lithium clavulanate Levocarnitine Levocarnitine impurity A Levodopa Levodropropizine Levodropropizine impurity A Levamisole for system suitability Levamisole hydrochloride Levamisole - reference spectrum Levocabastine hydrochloride Levocabastine impurity D Reference Standard © Council of Europe, all rights reserved 2006 L0720800 Y0000112 L0745000 L0750000 Y0000322 Y0000341 New Y0000688 Y0000603 Y0000604 Y0000605 L0750500 New Y0000576 New Y0000718 L0500000 L0505000 L0551000 L0570000 L0595000 L0600000 L0650000 L0655000 L0700000 L0702000 L0702100 L0720000 New L0399900 L0399905 L0400000 L0420000 L0420002 Order Code Y0000047 L0380000 Y0000048 L0390000 L0390008 Catalogue No. 48-2006/4 1 1 1 1 1 1 3 1 1 1 1 1 1 1 1 1 2 1 1 2 1 5 1 2 4 2 1 1 1 1 1 1 n/a 1 1 Batch 60 mg 50 mg 50 mg 150 mg 15 mg 20 mg 60 mg 20 mg 10 mg 50 mg 100 mg 0.8 mg 10 mg 100 mg 50 mg 30 mg 100 mg 50 mg 100 mg 250 mg 250 mg 50 mg 50 mg 2 mg 125 mg 100 mg 60 mg 20 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1339 1339 0038 1535 1535 0726,1728 0726 1728 1484 1484 Monograph Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 l 79 a 79 a 1189,1275 +5°C a 1988 +5°C a 0928 +5°C a 0921,0929,1729 +5°C g 0929 Yes +5°C g 1729 +5°C g 2124 +5°C a 2124 Yes +5°C a 2124 +5°C a 2124 +5°C a 1121 +5°C j 1121 +5°C j (5RS)-7-chloro-5-(2-chlorophenyl)-4,5-dihydro-1H-1,4-benzodia 1121 +5°C a zepine-2,3-dione 32 For extra charges please see 2.2 20303 0925,20303 0926 90.0% CŒ—HŒÕI÷NNaO÷ 0401,0728 0727,1362 0227,1242,1363 87.4% CŒ‡H–÷NœOÿS 0582,0583,0996 0772 98.7% CŒ—HŒŒI–NNaO÷ 0401,0728 1120 1120 98.8% C‡H‡LiNO—; 1 mg of CŸH‡LiNO— corresponds to 1.157 mg of 1140,1653 C‡H‡KNO— (2R)-3-(4-phenylpiperazin-1-yl)propane-1,2-diol (dextrodropropizine) Information Unit Sale Quantity Unit 80 mg 1 50 mg 1 n/a 1 125 mg 1 20 mg 1 1-[4-cyano-4-(4-fluorophenyl)cyclohexyl]-4-phenyl-4-piperidine carboxylic acid 125 mg 1 Batch 1 is valid until 30 April 2007 50 mg 1 4-(trimethylammonio)but-2-enoate 6 December 2006 1 n/a 2 4 M0100000 Y0000143 M0160000 M0200000 Measles vaccine (live) BRP Mebendazole Mebendazole for system suitability Mebendazole - reference spectrum Meclozine hydrochloride Medronic acid Medroxyprogesterone acetate Medroxyprogesterone acetate for performance test Medroxyprogesterone acetate for system suitability Mefenamic acid Mefloquine hydrochloride Megestrol acetate Megestrol acetate - reference spectrum Meglumine - reference spectrum Menadione Menthol Mepivacaine hydrochloride Mepivacaine impurity B Meprobamate - * psy Mepyramine maleate © Council of Europe, all rights reserved 2006 M0210000 M0215000 Y0000144 Y0000168 M0220000 M0240000 New M0250000 M0250010 Y0000598 M0252600 M0253000 M0260000 M0260100 Y0000267 M0300000 M0350000 M0370000 M0370020 M0400000 M0500000 M0206000 Maprotiline hydrochloride M0206040 Maprotiline impurity D 1 1 1 n/a 1 1 2 2 1 1 1 2 n/a n/a 1 4 1 1 1 1 1 1 2 M0120010 Malathion impurity B Maleic acid Malic acid - reference spectrum Maltitol Mannitol 1 1 2 M0088000 Magnesium aspartate dihydrate M0120000 Malathion M0120005 Malathion impurity A Batch 2 1 2 2 Reference Standard Lovastatin Lynestrenol Lysine acetate Lysine hydrochloride Order Code L0790000 L0800000 Y0000397 L0900000 Catalogue No. 48-2006/4 80 mg 20 mg 20 mg n/a 150 mg 20 mg 100 mg 50 mg 10 mg 50 mg 100 mg 50 mg n/a n/a 100 mg 150 mg 100 mg 60 mg 100 mg 1000 mg 100 mg 25 mg 100 mg n/a 1200 mg 1200 mg 10 mg 60 mg 250 mg 10 mg 5 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 33 (¢£)-N-(2,6-dimethylphenyl)piperidine-2-carboxamide Batch 1 is valid until 31 March 2007 3-(9,10-dihydro-9,10-ethanoanthracen-9-yl)-N-methylprop-2en-1-amine; (dehydromaprotiline) 4.3 logŒÕ (ie 20000) infective viral units per vial 99.8% CŒœHœ÷OŒŒ ; Batch 1 is valid until 31 December 2006 98.6% CÿHŒ÷Oÿ 99.3% CŒÕHŒ„OÿPSœ diethyl (2RS)-2-[(methoxy)(methylsulfanyl)-S-phosphinothioyl] butane dioate (isomalathion) diethyl (2RS)-2-(dimethoxy-S-phosphinothioyl)-butanedioate (maloxon) Information Unit Sale Quantity Unit 40 mg 1 99.7% Cœ÷H–ÿO— ; Batch 1 is valid until 31 October 2006 50 mg 1 60 mg 1 50 mg 1 Batch 1 is valid until 30 September 2006 Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C Leaflet Storage c a a l a a a a c a a a l l a a a a j a a a a l a a c a a c 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 90 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 c 79 a 79 a 79 a For extra charges please see 2.2 1057,0213 1208,1254 0845 0845 0622 0641 0673,1094,1593 0673 0673 1240 1241 0673,1593 1593 2055 0507 0619,0623 1242 1242 0407,1689 0278 0365,0925 2080 1235,1236 0435,0559,1381, 1531 1237 1237 1343 1538,1563 0558 2114 0805,0806,0930, 1654 1445 1343 1343 Monograph 6 December 2006 n/a n/a n/a n/a 50 mg 50 mg 100 mg 20 mg 10 mg n/a n/a n/a n/a 1 1 4 1 2 1 New Y0000664 Methotrexate impurity E © Council of Europe, all rights reserved 2006 3 n/a n/a M1100000 3-Methoxymethyldopa 200 mg n/a 1 n/a 20 mg 10 mg n/a n/a 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 34 4-[[(2-amino-4hydroxypteridin-6-yl)methyl]methyl-amino] benzoic acid 4-[[(2,4-diaminopteridin-6-yl)methyl]methylamino]benzoic acid (4-amino-N10-methylpteroic acid, APA) 88.6% CœÕHœœN‡O— ; Batch 3 is valid until 28 February 2006 Information Unit Sale Quantity Unit 10 mg 1 N-(4-methoxybenzyl)pyridin-2-amine 10 mg 1 125 mg 1 n/a 1 10 mg 1 2-(acetylsulphanyl)ethanesulphonic acid 10 mg 1 2,2'-disulphanediyl)bis(ethanesulphonic acid) 0.5 mg 1 60 mg 1 99.3% CœÕH–œOœ 30 mg 1 17ß-hydroxy-1alpha-methylandrost-4-en-3-one 100 mg 1 n/a 1 100 mg 1 100 mg 1 Batch 2 is valid until 30 April 2007 10 mg 1 4-formylamino-1,5-dimethyl-2-phenyl-1,2-dihydro-3§-pyrazol3-one 50 mg 200 mg n/a 1 1 1 n/a 1 1 1 1 1 1 n/a 3 3 2 Batch 2 1 n/a Mepyramine impurity A Mepyramine impurity C Mesalazine Mesna - reference spectrum Mesna impurity C Mesna impurity D Meso-rich exametazime Mesterolone Mesterolone impurity A Mestranol Metacresol - reference spectrum Metacycline hydrochloride Metamizole sodium Metamizole impurity A Reference Standard M0605000 Metformin hydrochloride New Y0000770 Methacrylic acid-ethyl acrylate copolymer (1:1) - type A M0610000 Methacrylic acid-ethylacrylate copolymer(1:1) - reference spectrum M0610030 Methacrylic acid-ethyl acrylate copolymer (1:1), dispersion 30%-ref.sp Y0000323 Methacrylic acid-ethyl acrylate copolymer (1:1) - type B M0620000 Methacrylic acid-methylmethacrylate copolymer(1:1)reference spectrum M0630000 Methacrylic acid-methylmethacrylate copolymer(1:2)reference spectrum M0800000 Methadone hydrochloride - reference spectrum Y0000428 Methanol - reference spectrum M0900000 Methaqualone - reference spectrum M0920001 Methenamine - reference spectrum M0950000 DL-Methionine M0960000 Methionine M1000000 Methotrexate Y0000602 Methotrexate for peak identification M1000008 Methotrexate impurity D Order Code New Y0000679 New Y0000680 Y0000297 Y0000337 Y0000316 Y0000317 Y0000227 Y0000097 Y0000096 M0600000 Y0000301 M0600500 New M0600900 M0600905 Catalogue No. 48-2006/4 0045 0560 Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a g l l l l a a g g g l a l l a a l 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 g 79 a 79 l 79 a 79 a 79 a 79 a 79 a 79 a 79 l 79 a 79 a 79 a For extra charges please see 2.2 0408,1787 1989 0510 1545 0624 0788,1027 0560 0560 0560 1130 1128 1127 1129 0931 1128 1128 0278 0278 1699,1993 1674 1674 1674 1925 1730 1730 0509 2077 0272,0820 1346 1346 Monograph 6 December 2006 1 1 4 1 1 1 3 2 1 2 1 1 2 1 1 1 n/a 2 1 1 2 1 1 2 1 1 2 1 Methylatropine bromide Methylatropine nitrate Methylcarbidopa Methyl 2-(4-chlorophenoxy)-2-methylpropionate Methyldopa Methylene chloride 2-(1-Methylethyl) pentanoic acid Methyl 12-hydroxystearate Methyl nicotinate Methylnitrosoindoline Methyl parahydroxybenzoate Methylphenobarbital - * psy Methylprednisolone Methylprednisolone acetate Methylprednisolone hydrogen succinate Methylprednisolone hydrogen succinate for performance test N-Methylpyrrolidone - reference spectrum Methyl ricinoleate Methylrosanilinium chloride Methylrosanilinium for system suitability Methyl stearate Methyltestosterone Methylthioninium chloride Methylthioninium impurity A Metixene hydrochloride Metoclopramide Metoclopramide hydrochloride Metoclopramide impurity A Metoprolol succinate - reference spectrum Metoprolol tartrate Metrifonate Metronidazole Metronidazole benzoate Metronidazole benzoate - reference spectrum © Council of Europe, all rights reserved 2006 Y0000171 M1830000 M1845000 New M1850000 M1851000 Y0000069 n/a 1 1 2 1 n/a 1 1 Batch Reference Standard M1825010 Metoclopramide impurity E Y0000145 Metoprolol impurity A Order Code M1300000 M1400000 M1450000 M1470000 M1500000 M1550000 M1551000 M1556000 Y0000398 New M1625000 M1650000 M1700000 M1750000 M1755000 M1755200 M1755220 Y0000190 M1770180 Y0000418 Y0000407 M1770200 M1800000 M1800900 M1800902 M1808000 M1824990 M1825000 M1824995 Catalogue No. 48-2006/4 n/a 60 mg 100 mg 50 mg 50 mg n/a 1 1 1 1 1 1 35 Batch 1 is valid until 31 March 2007 Information Unit Sale Quantity Unit 100 mg 1 100 mg 1 1 mg 1 0.5 ml 1 50 mg 1 2 ml 1 25 mg 1 100 mg 1 Batch 1 is valid until 31 January 2006 25 mg 1 100 mg 1 Batch 1 is valid until 30 April 2007 100 mg 1 500 mg 1 150 mg 1 100 mg 1 125 mg 1 50 mg 1 n/a 1 125 mg 1 Batch 1 is valid until 31 March 2006 40 mg 1 10 mg 1 100 mg 1 100 mg 1 50 mg 1 methylene blue 20 mg 1 3-(dimethylamino)-7-(methylamino)phenothiazin-5-ylium 75 mg 1 100 mg 1 50 mg 1 25 mg 1 4-(acetylamino)-5-chloro-N-(2-diethylaminoethyl)-2-methoxy benzamide 20 mg 1 N,N-diethylethane-1,2-diamine 10 mg 1 (2RS)-1-(ethylamino)-3-[4-(2-methoxyethyl)phenoxy]propan2-ol Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage l a a a a l g a 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 j 79 a 79 a 79 a 79 a 79 l 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a For extra charges please see 2.2 1448 1028 1133 0675,0934 1424 0934 1575 1028,1448 0511,0919 0512 0755 0318 0045,0755 0932 0678,1378 1497 2129 1108 0409,1262,2134 0189 0312,0388,0561 0933 0768,1131 1131 1675 0051 1990 1990 0051,1497 0410 1132 1132 1347 1348 0674,0856,1303 1348 Monograph 6 December 2006 M3600000 Mumps vaccine (live) BRP M3805000 Mupirocin - reference spectrum M3805500 Mupirocin calcium - reference spectrum M3806000 Mupirocin lithium © Council of Europe, all rights reserved 2006 1 n/a n/a 1 1 1 1 1 2 1 1 1 1 Modafinil Modafinil for system suitability Molgramostim Mometasone furoate Morantel hydrogen tartrate Morphine hydrochloride (trihydrate) - * narc Morphine sulphate - * narc Moxonidine Moxonidine impurity A Y0000635 Y0000636 Y0000251 M2900000 Y0000028 Y0000451 Y0000452 Y0000226 Y0000222 2 1 1 2 1 1 1 1 2 3 Midazolam - * psy Milk thistle standardised dry extract Midazolam for system suitability - * psy Minocycline hydrochloride Minoxidil Misoprostol Misoprostol impurity A M2200000 Y0000539 Y0000599 M2280000 M2300000 Y0000490 Y0000491 1 1 1 1 1 2 1 1 Batch Y0000378 Mitomycin M2305000 Mitoxantrone hydrochloride M2305005 Mitoxantrone impurity A Mexiletine impurity D Mianserin hydrochloride Miconazole Miconazole nitrate Midazolam impurity C Y0000203 M1875000 M1880000 M1900000 Y0000562 Order Reference Standard Code New Y0000087 Metronidazole impurity A M1860000 Mexiletine hydrochloride Y0000202 Mexiletine impurity C Catalogue No. 48-2006/4 33 mg n/a n/a 100 mg 110 mg 0.1 mg 0.3 ml 100 mg 50 mg 10 mg 40 mg 50 mg 10 mg 120 mg 60 mg 5 mg 50 mg 120 mg 1 mg 125 mg 50 mg 30 mg 5 mg 50 mg 70 mg 100 mg 0.08 mg 5 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 36 95.4% CœÿH÷–O„Li 99.7% C„HŒœClN—O 4,6-dichloro-N-(4,5-dihydro-1H-imidazol-2-yl)-2-methyl-5pyrimidinamine 4.6 logŒÕ (ie40000) infective viral units per vial 13.45 mg protein per ml 99.2% CœœH–‡O— mixture of methyl 7-[(1RS,2SR, 3SR)-3-hydroxy-2-[(1E,4RS)-4-hydroxy-4-methyloct1-enyl]-5-ox ocyclopentyl]heptanoate and methyl 7-[(1RS,2SR,3SR)-3-hydroxy-2-[(1E,4SR)-4-hydroxy4-methyloct -1-enyl]-5-oxocyclopentyl]heptanoate (8-epimisoprostol), 99.1% CŒ—HŒ‡N÷O— 97.8% CœœH–ÕClœN÷Oÿ 1-amino-5,8-dihydroxy-4-[[2-[(2-hydroxyethyl)amino]ethyl] amino]anthracene-9,10-dione ; Batch 2 is valid until 31 March 2006 100.0% CŒ—HŒ—NOœS 90.8% Cœ–Hœ‡ClN–OŸ 27.5% of silibinin (A+B) acide 8-chloro-6-(2-fluorophenyl)-1-methyl-4H-imidazo[1,5-a] [1,4]benzodiazepine-3-carboxylique Information Unit Sale Quantity Unit 10 mg 1 2-methyl-4-nitroimidazole ; Batch 1 is valid until 30 April 2007 100 mg 1 2 mg 1 1,1'-[(3,3',5,5'-tetramethylbiphenyl-4,4'-diyl)bisoxy] dipropan-2-amine 2 mg 1 (2RS)-2-(2,6-dimethylphenoxy)propan-1-amine Yes +5°C +5°C -80°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a d a a k k a a g a a j c j a a g c a a a a a 79 79 79 90 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 0538,1057 Yes -80°C d 1450 l 1451 l 1450,1451 +5°C a For extra charges please see 2.2 2307 2307 1641 1449 1546 0097 1244 1758 1758 1655 1243 1243 0936,1065 2071 0936 1030 0937 1731 1731 1029 0846 0935,1335 0513,1148 0936 0675 1029 1029 Monograph 6 December 2006 Naproxen Naproxen (racemic) Naproxen impurity L Neamine © Council of Europe, all rights reserved 2006 N0250000 Y0000399 Y0000631 N0300000 Nalidixic acid Naloxone hydrochloride dihydrate Naloxone impurity A Naloxone for peak identification Naltrexone hydrochloride Naltrexone impurity C Nandrolone decanoate Nandrolone decanoate for peak identification Nandrolone decanoate for system suitability Naphazoline hydrochloride Naphazoline hydrochloride - reference spectrum Naphazoline nitrate Naphazoline impurity A 1 1 1 3 1 1 2 1 1 1 1 1 1 3 n/a 2 3 1 Y0000331 Naftidrofuryl impurity F N0050000 N0075000 N0075005 New Y0000695 Y0000400 Y0000410 Y0000542 Y0000547 Y0000548 N0080000 Y0000252 N0100000 N0200000 1 Y0000122 Naftidrofuryl impurity C 1 2 1 1 1 1 1 1 1 2 1 1 n/a 1 Batch 1 Mycophenolate mofetil Mycophenolate mofetil for peak identification Mycoplasma fermentans BRP Mycoplasma hyorhinis BRP Mycoplasma orale BRP Mycoplasma synoviae BRP Myo-inositol Nabumetone Nabumetone impurity D Nabumetone impurity F Nadolol Nadroparin calcium Naftidrofuryl - reference spectrum Naftidrofuryl impurity A Reference Standard Y0000121 Naftidrofuryl impurity B Order Code Y0000489 Y0000519 Y0000692 Y0000690 Y0000691 Y0000689 Y0000485 N0020000 N0020020 N0020030 Y0000146 N0025000 Y0000077 Y0000120 Catalogue No. 48-2006/4 100 mg 10 mg 10 mg 0.5 mg 100 mg 100 mg 10 mg 10 mg 50 mg 15 mg 5 mg 10 mg 10 mg 50 mg n/a 10 mg 25 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1594 1594 1594 1700 1700 20607 20607 20607 20607 1805 1350 1350 1350 1789 0828,1134 1594 1594 Monograph 37 90.0% CŒŒHœÿN÷Oÿ Yes Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -80°C -80°C -80°C -80°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a a a c c c a l a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 120 d 120 d 120 d 120 d 79 a 79 a 79 a 79 a 79 a 79 a 79 l 79 a For extra charges please see 2.2 0731 0731 1702 0180,0197 0701 0729,2099 4,5¶-epoxy-3,14-dihydroxymorphinan-6-one (noroxymorphone) 0729 0729 1790 N-(3-butenyl)-noroxymorphone 1790 1992 1992 1992 1162 0730 0147 N-(2-aminoethyl)-2-(naphthalen-1-yl)acetamide 0147,0730 (naphthylacetylethylenediamine) Information Unit Sale Quantity Unit 30 mg 1 10 mg 1 Batch 1 is valid until 30 June 2006 1 ml 1 1 ml 1 1 ml 1 1 ml 1 1020 mg 1 99.8% CÿHŒœOÿ 60 mg 1 99.8% CŒ—HŒÿOœ 10 mg 1 (E)-4-(6-methoxynaphthalen-2-yl)but-3-en-2-one 10 mg 1 6,6'-dimethoxy-2,2'-binaphthalenyl 100 mg 1 250 mg 1 n/a 1 10 mg 1 2-[(naphtalen-1-yl)methyl]-3-(tetrahydrofuran-2-yl)propanoic acid 25 mg 1 98% CœÕHœ–O–; ethyl 2-[(naphtalen-1-yl)methyl]3-(tetrahydrofuran-2-yl)propanoate 50 mg 1 97.5% C–ÕH––NOœ; 2-(diethylamino)ethyl 3-[(naphtalen-1-yl)2-[(naphtalen-1-yl)methyl]propanoate 10 mg 1 2-[(diethylamino)ethyl 2-[(naphthalen-2-yl)methyl]-3(tetrahydrofuran-2-yl)propanoate 6 December 2006 3 2 1 1 1 1 1 1 N0400000 Neomycin sulphate N0401000 N0500000 N0550000 N0559000 Y0000520 Y0000521 Y0000388 1 1 n/a 2 1 1 1 N0560000 N0600000 N0590000 N0590200 N0700000 N0750000 N0750010 © Council of Europe, all rights reserved 2006 N0900000 Nitrazepam - * psy N0900010 Nitrazepam impurity A 1 1 n/a 1 1 1 1 2 2 Y0000178 N0800000 N0845000 N0845006 N0845008 N0850000 N0850010 Nifuroxazide - reference spectrum Nikethamide Nimesulide Nimesulide impurity C Nimesulide impurity D Nimodipine Nimodipine impurity A 1 N0750015 Nifedipine impurity B Niclosamide (anhydrous) Nicotinamide Nicotine - reference spectrum Nicotine ditartrate Nicotinic acid Nifedipine Nifedipine impurity A n/a 1 Y0000287 Nicergoline - reference spectrum Y0000283 Nicergoline impurity A Neomycin sulphate for microbiological assay Neostigmine bromide Neostigmine metilsulfate Netilmicin sulphate Nevirapine (anhydrous) Nevirapine for peak identification Newcastle Disease Vaccine (inactivated) BRP 1 1 Batch Order Reference Standard Code N0399000 Neohesperidin-dihydrochalcone N0399004 Neohesperidin-dihydrochalcone impurity B Catalogue No. 48-2006/4 100 mg 25 mg n/a 1 ml 100 mg 25 mg 20 mg 50 mg 1 ml 20 mg 50 mg 50 mg n/a 20 mg 100 mg 50 mg 20 mg n/a 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 38 3-amino-6-nitro-4-phenylquinol-2-one 2-methoxyethyl 1-methylethyl 2,6-dimethyl-4-(3-nitrophenyl) pyridine-3,5-dicarboxylate 2-phenoxyaniline 4-nitro-2-phenoxyaniline Dimethyl 2,6-dimethyl-4-(2-nitrophenyl)pyridine-3,5dicarboxylate Dimethyl 2,6-dimethyl-4-(2-nitrosophenyl)pyridine-3,5dicarboxylate 92.6% CŒÕHŒ÷Nœ x 2 C÷HÿOÿ [(6aR,9R,10aS)-10a-methoxy-4,7-dimethyl-4,6,6a,7,8,9,10,10aoctahydroindol[4,3-fg]quinolin-9-yl]methyl 5-chloropyridine-3-carboxylate Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C -20°C +5°C +5°C -20°C -20°C -20°C +5°C Leaflet Storage j a l a a a a a a a a a l a a a a l a a a a a g g c a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 180 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 0415,0898,1121 0415 1999 0233 1548 1548 1548 1245 1245 0627 0679,0680 0047 1452,1792 1452,1792 0459,0859 0627,1013 0627 1998 1998 Information Unit Sale Monograph Quantity Unit 125 mg 1 89.9% Cœ‡H–ÿOŒ— 1547 10 mg 1 89% Cœ‡H–œOŒ—; 7-[[2-O-(6-deoxy-¶-L-mannopyranosyl) 1547 -ß-D-glucopyranosyl]oxy]-5-hydroxy-2-(3-hydroxy-4-methoxyph enyl)-4H-1-benzopyran-4-one (neodiosmin) 50 mg 1 Not to be used for microbiological assay 0032,0033,0053, 0180,0197,0485, 0645 19850 IU per vial ; Batch 1 is valid until 31 December 2005 25 mg 1 0197,20702 50 mg 1 0046 50 mg 1 0626 25 mg 2 14656 IU per vial 1351,20702 99.8% CŒ—HŒ÷N÷O 30 mg 1 2255 0.058 mg 1 2255 4 uc 1 The kit contains :1 vial BRP1 NDV reference antigen, 1 vial BRP1 0870 NDV control antigen, 1 vial BRP1 NDV coating antibody, 1 vial BRP1 NDV conjugated, detection antibody 6 December 2006 Nomegestrol acetate Nomegestrol acetate impurity A Nonivamide Nonoxinol 9 - reference spectrum Noradrenaline tartrate Noradrenaline impurity D N1080000 N1080005 Y0000670 N1084000 N1100000 New Y0000681 Norgestrel Norpseudoephedrine hydrochloride - * psy Nortriptyline hydrochloride Noscapine Nystatin Octoxinol 10 Octyl gallate Octyldodecanol Ofloxacin Ofloxacin impurity A © Council of Europe, all rights reserved 2006 N1250000 N1279000 N1280000 N1300000 N1400000 O0100900 Y0000368 O0101000 O0120000 O0120010 New Y0000682 Noradrenaline impurity E New Y0000686 Noradrenaline impurity F N1130000 Norcyclobenzaprine N1140000 Nordazepam -* psy New N1200000 Norethisterone N1225000 Norethisterone acetate Y0000522 Norethisterone for system suitability N1230000 Norfloxacin N1230010 Norfloxacin impurity A n/a 1 1 n/a 1 1 Nitric oxide - reference spectrum Nitrofural Nitrosotriaminopyrimidine Nitrous oxide - reference spectrum Nizatidine Nizatidine impurity F N0930000 N0950000 N1000000 N1050000 N1090000 N1090060 1 2 2 1 4 2 1 4 1 1 1 1 1 1 2 1 1 1 1 1 1 1 n/a 4 1 2 2 Batch Order Reference Standard Code N0905000 Nitrendipine N0905005 Nitrendipine impurity A Catalogue No. 48-2006/4 30 mg 50 mg 10 mg 100 mg 300 mg 300 mg 30 mg 400 mg 50 mg 20 mg 10 mg 10 mg 25 mg 50 mg 100 mg 100 mg 10 mg 50 mg 20 mg 100 mg 50 mg 10 mg n/a 200 mg 15 mg n/a 100 mg 50 mg n/a 250 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1246 1246 Monograph 39 (RS)-9,10-difluoro-3-methyl-7-oxo-2,3-dihydro-7H-pyrido [1,2,3-de][1,4]benzoxazine-6-carboxylic acid (FPA) 94.8% CœÕH÷œO 5600 IU per mg C÷ŸHŸ—NOŒŸ Cathine 7-chloro-1-ethyl-6-fluoro-4-oxo-1,4-dihydroquinoline-3carboxylic acid (corresponding also to pefloxacin impurity F) Dipotassium clorazepate impurity B Batch 1 is valid until 31 May 2007 Yes Yes +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a j a a c a a a a a a a a j a a c a a a a g l g g l a a l a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 0940 0683 0941 0102,0515,0516 0517,1292,20702 1553 2057 1136 1455 1455 0941 0898,1466 0234,1212 0850 0234 1248 1248,1460 1551 1551 2336,2337 1454 0254,0285,0732 4[(1R)-2-amino-1-methoxyethyl]benzene-1,2-diol (noradrenaline 0285,0732 methyl ether) 2-chloro-1-(3,4-dihydroxyphenyl)ethanone 0285,0732 N-benzyl-1-phenylmethanamine 0285,0732 17¶-acetoxy-6¶-methyl-19-norpregn-4-ene-3,20-dione 99.1% CŒŸHœŸNO– 1550 1135 0058 0416 99.3% CŒœHœŒN—OœSœ 1453 (EZ)-NÁ,NÁ'-[thiazole-2,4-diylbis(methylenesulphanediylethylene)] 1453 bis(N'-methyl-2-nitroethene-1,1-diamine) 99.8% CÿHÿN÷O÷ Information Unit Sale Quantity Unit 60 mg 1 20 mg 1 ethyl methyl-2,6-dimethyl-4-(3-nitrophenyl)pyridine-3,5dicarboxylate; (nitrophenylpyridine analogue) 6 December 2006 Oxfendazole for veterinary use Oxfendazole impurity B Oxfendazole with impurity D Oxitropium bromide © Council of Europe, all rights reserved 2006 O0225800 Y0000224 Y0000225 New Y0000709 2 1 1 1 1 1 1 1 1 O0225000 Y0000543 Y0000350 Y0000404 Y0000390 Oxazepam - * psy Oxazepam for peak identification - * psy Oxeladin hydrogen citrate Oxeladin impurity C Oxeladin impurity D 1 Y0000274 Oxaliplatin impurity D 1 1 1 2 3 2 Ouabain Oxacillin sodium monohydrate Oxacillin for peak identification Oxaliplatin Oxaliplatin impurity B O0200000 Y0000638 Y0000560 Y0000271 Y0000272 1 1 2 2 2 1 1 2 2 1 1 1 2 Batch Y0000273 Oxaliplatin impurity C Olsalazine sodium Olsalazine sodium for performance test Omeprazole Omeprazole impurity D Ondansetron hydrochloride dihydrate Ondansetron for LC system suitability Ondansetron for TLC system suitability Ondansetron impurity D Orciprenaline sulphate Orphenadrine citrate Orphenadrine hydrochloride Orphenadrine impurity E O0146000 O0146010 O0150000 O0151000 Y0000218 Y0000197 Y0000196 Y0000195 O0180000 Y0000101 Y0000100 Y0000102 Order Reference Standard Code New O0120050 Ofloxacin impurity E Catalogue No. 48-2006/4 50 mg 10 mg 10 mg 50 mg 50 mg 0.008 mg 50 mg 10 mg 20 mg 5 mg 10 mg 150 mg 110 mg 10 mg 250 mg 20 mg 60 mg 60 mg 50 mg 5 mg 200 mg 10 mg 30 mg 10 mg 100 mg 100 mg 100 mg 30 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 40 methyl [5-(phenylsulphonyl)-1H-benzimidazole-2-yl]carbamate 2-(diethylamino)ethyl 2-ethyl-2-phenylbutanoate 2-(2-diethylaminoethoxy)ethyl 2-phenyl-butyrate dihydrogen citrate 99.8 % C‡HŒ÷NœO÷Pt ; Batch 1 is valid until 28 February 2007 (SP-4-2)-diaqua[(1R,2R)-cyclohexane-1,2-diamine-kN,kN'] platinum (diaquodiaminocyclohexaneplatinum) ; Batch 2 is valid until 31 October 2006 (OC-6-33)-[(1R,2R)-cyclohexane-1,2-diamine-kN,kN'][ethanedioato(2-)-kOÁ,kOË]dihydroxyplatinum ; Batch 1 is valid until 31 July 2006 (SP-4-2)-[(1S,2S)-cyclohexane-1,2-diamine-kN,kN'][ethanedioato(2-)-kOÁ,kOË]platinum (S,S-enantiomer of oxaliplatin) (RS)-N,N-dimethyl-2-[(3-methylphenyl)phenylmethoxy] ethanamine (meta-methylbenzyl isomer) 80.0% Cœ„H÷÷OŒœ 93.8% CŒ„HŒ‡N–NaO—S 9-methyl-3-methylene-1,2,3,9-tetrahydro-4H-carbazol-4-one Batch 1 is valid until 31 January 2007 Omeprazole sulphone 89.8% CŒ‡HœÕClN–O Information Unit Sale Quantity Unit 20 mg 1 (RS)-9-fluoro-3-methyl-10-(piperazin-1-yl)-7-oxo-2,3-dihydro7H-pyrido[1,2,3-de][1,4]benzoxazine-6-carboxylic acid ; Batch 1 is valid until 31 March 2007 1458 1458 1458 2170 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a j j g g g g g a a a g g a a c c g g g g a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0778,1191 0778 1761 1761 1761 2017 2017 0048 2260 2260 2017 2017 1457 1457 0942,1032 0942,1032 2016 2016 2016 2016 1033,1332 1759 1760 1759,1760 1455 Monograph 6 December 2006 1 1 1 1 2 O0250000 O0260000 O0270000 O0288000 O0288005 Pancreas powder (protease) BRP Pancuronium bromide Pancuronium bromide for system suitability Papaverine hydrochloride Paracetamol Paraffin, hard - reference spectrum Paraffin, liquid - reference spectrum Paraffin (white soft) - reference spectrum Paraffin, yellow soft - reference spectrum Parnaparin sodium P0200000 P0250000 Y0000577 P0270000 P0300000 P0302000 Y0000058 Y0000293 P0302500 P0305000 © Council of Europe, all rights reserved 2006 Oxymetazoline hydrochloride Oxyphenbutazone Oxytetracycline Oxytetracycline hydrochloride Oxytocin Oxytocin/Desmopressin validation mixture Palmitic acid Pamidronate disodium pentahydrate Pancreas powder (amylase and lipase) BRP O0290000 O0300000 O0400000 New O0500000 O0700000 O0770000 P0090000 Y0000524 P0100000 Y0000492 Oxycodone hydrochloride - * narc Y0000453 Oxycodone impurity D 3 1 1 1 2 n/a n/a n/a n/a 1 1 1 6 4 3 2 3 1 3 1 1 1 1 1 O0240000 Oxolinic acid O0240005 Oxolinic acid impurity A O0240010 Oxolinic acid impurity B Oxprenolol hydrochloride Oxybendazole Oxybuprocaïne hydrochloride Oxybutynin hydrochloride Oxybutynin impurity A 1 1 Batch Y0000713 Oxitropium bromide impurity D Order Reference Standard Code New Y0000715 Oxitropium bromide impurity B Catalogue No. 48-2006/4 2000 mg 100 mg 20 mg 25 mg 100 mg n/a n/a n/a n/a 250 mg 80 mg 100 mg 100 mg 20 mg 41 mg 0.2 mg 100 mg 10 mg 2000 mg 100 mg 25 mg 50 mg 100 mg 150 mg 150 mg 10 mg 50 mg 20 mg 20 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0943 0418 0198,0199 0198,1030 0779,0780 0712,0779,0780 0229,0882,2058 1779 0350 1793 1793 0628,0876,1072 1386 1251 1354 1354 1353 1353 1353 41 +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a g g a a l l l l a a a a a c c a a a k a a a a a a a a a g 79 79 79 79 79 79 79 79 79 79 79 79 79 79 90 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 41.4 Ph. Eur. U. lipolytic activity per mg; 56.3 Ph. Eur. U. amylolytic activity per mg ; Batch 2 is valid until 31 October 2006 1.48 Ph. Eur. U. per mg ; Batch 2 is valid until 31 October 2006 0350 Vecuronium impurity B 0681,1769 0681 0102,0573 0049 1034 0239,0240 1799 1554 0828,1252 90.2% CœœHœ÷NœO„ ; Batch 5 is valid until 31 December 2005 Batch 3 is valid until 31 March 2007 1.24 mg per vial of C÷–HÿÿNŒœOŒœSœ about 0.1 mg oxytocin + 0.1 mg desmopressin per vial Batch 2 is valid until 31 March 2006 7,8-didehydro-4,5 alpha-epoxy-14-hydroxy-3-methoxy -17-methylmorphinan-6-one (14-hydroxycodeinone) 4-(diethylamino)but-2-ynyl(¢£)-2-(cyclohex-3-enyl)-2cyclohexyl-2-hydroxyacetate 8-hydroxy-1,3-dioxolo[4,5-g]quinoline-7-carboxylic acid ethyl 5-ethyl-8-oxo-5,8-dihydro-1,3-dioxolo[4,5-g]quinoline-7carboxylate Information Unit Sale Monograph Quantity Unit 15 mg 1 (1R,2R,4S,5S,7s)-7-[[(2S)-3-hydroxy-2-phenylpropanoyl]oxy]-9, 2170 9-dimethyl-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane (methylhyoscine) 10 mg 1 (1R,2R,4S,5S,7s,9r)-9-ethyl-9-methyl-7-[(2-phenylprop-2-enoyl) 2170 oxy]-3-oxa-9-azoniatricyclo[3.3.1.02,4]nonane (apo-N-ethylhyoscine) 6 December 2006 1 2 1 1 1 1 1 Y0000579 Paroxetine hydrochloride (anhydrous) impurity C Y0000256 Paroxetine impurity D Y0000580 Paroxetine impurity E Y0000581 Y0000630 P0309000 P0309020 1 1 1 1 n/a n/a n/a 1 1 n/a 1 1 Penicillamine Penicillamine disulphide Pentaerythrityl tetranitrate diluted Pentamidine diisetionate Pentazocine - reference spectrum Pentazocine hydrochloride - reference spectrum Pentazocine lactate - reference spectrum Pentobarbital - * psy Pentoxifylline Pentoxyverine hydrogen citrate - reference spect. Pentoxyverine impurity A Pentoxyverine impurity B Pepsin powder BRP Pergolide mesilate Perindopril impurity A Perindopril for stereochemical purity Perindopril for system suitability P0310000 P0320000 P0400100 P0405000 P0405500 P0405510 Y0000417 P0500000 P0510000 Y0000076 Y0000098 Y0000099 P0525000 Y0000010 Y0000237 Y0000207 Y0000206 © Council of Europe, all rights reserved 2006 1 1 P0307000 Penbutolol sulphate P0307005 Penbutolol impurity A 2 1 1 1 1 2 P0309030 Pefloxacin impurity C Paroxetine hydrochloride (anhydrous) impurity H Paroxetine for system suitability Pefloxacin mesilate dihydrate Pefloxacin impurity B 1 1 2 Batch Order Reference Standard Code Y0000578 Paroxetine hydrochloride (anhydrous) Y0000281 Paroxetine hydrochloride hemihydrate Y0000233 Paroxetine impurity A Catalogue No. 48-2006/4 2000 mg 150 mg 10 mg 40 mg 30 mg 100 mg 100 mg 600 mg 30 mg n/a n/a n/a 500 mg 100 mg n/a 10 mg 10 mg 100 mg 20 mg 0.01 mg 5 mg 200 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 42 1-phenylcyclopentanecarboxylic acid 2-(diethylamino)ethyl 1-phenylcyclopentanecarboxylate (caramiphen) 0.99 Ph. Eur. U. per mg 99.9% CœÕH–ÕNœO–Sœ (2S,3aS,7aS)-octahydro-1Hindole-2-carboxylic acid 10.0% C—H‡N÷OŒœ (2S)-1-[2-(cyclopent-1-enyl)phenoxy]-3-[(1,1-dimethylethyl) amino]propan-2-ol 1-ethyl-6-chloro-7-(4-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (chlorinated homologue of pefloxacin) 1-ethyl-6-fluoro-5-(4-methylpiperazin-1-yl)-4-oxo-1,4-dihydroquinoline-3-carboxylic acid (isopefloxacin) Information Unit Sale Quantity Unit 100 mg 1 100 mg 1 97.4% CŒ„HœŒClFNO– 5 mg 1 (3S,4R)-3-[[1,3-benzodioxol-5-yloxy]methyl]-4-phenylpiperidine (desfluoroparoxetine) 10 mg 1 (3S,4R)-3-[(1,3-benzodioxol-5-yloxy)methyl]-1-benzyl-4-(4-fluorophenyl)piperidine (N-benzylparoxetine) 5 mg 1 (3R,4S)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4-fluorophenyl) piperidine ((+)-trans-paroxetine) ; Batch 1 is valid until 31 July 2006 5 mg 1 (3RS,4RS)-3-[(1,3-benzodioxol-5-yloxy)methyl]-4-(4fluorophenyl)piperidine (cis-paroxetine) 10 mg 1 [(3S,4R)-1-benzyl-4-(4-fluorophenyl)piperidin-3-yl]methanol 0682 1555 2019 2019 2019 Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a h a l l l j a l a a a a a g g a a g g g 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 g 79 g 79 g For extra charges please see 2.2 0566 0566 1355 1137,1436 1462 1463 2000 0200,0419 0851 1621 1621 1621 1461 1461 1460 2283 2018 1460 1460 2283 2018,2283 2283 2283 2018,2283 2018,2283 Monograph 6 December 2006 Y0000123 Pidolic acid P1650000 Pilocarpine hydrochloride © Council of Europe, all rights reserved 2006 trans-Epoxyphytomenadione Picotamide monohydrate Picotamide impurity A Pidolate impurity B Phentolamine mesilate - reference spectrum Phenylalanine Phenylbutazone Phenylbutazone impurity B Phenylephrine Phenylephrine hydrochloride Phenylephrine hydrochloride for peak identification Phenylmercuric acetate - reference spectrum Phenylmercuric borate - reference spectrum Phenylpropanolamine hydrochloride - * Drug Precursor Phenytoin Phenytoin sodium Phloroglucinol (anhydrous) Pholcodine - reference spectrum Phthalylsulfathiazole Physostigmine salicylate Physostigmine sulphate Phytomenadione P1109000 P1150000 P1200000 Y0000147 P1240000 P1250000 New Y0000683 Y0000229 P1255100 P1260000 P1290000 P1300000 Y0000493 P1400000 P1500000 P1600000 P1605000 P1609000 P1609010 P1645000 P1645005 Y0000124 Perindopril tert-butylamine Perphenazine Pertussis toxin BRP Pethidine hydrochloride - reference spectrum Pethidine impurity A Phenazone Pheniramine maleate Phenobarbital - * psy Phenoxyethanol Phenoxymethylpenicillin Phenoxymethylpenicillin potassium Reference Standard Order Code Y0000238 P0550000 Y0000021 P0600000 P0600002 P0800000 New P0850000 New P0900000 P0950000 P1000000 P1100000 Catalogue No. 48-2006/4 1 1 2 1 1 1 n/a 3 1 1 1 2 1 n/a n/a 1 1 1 1 n/a 1 1 1 3 2 1 1 n/a 1 1 2 3 2 2 3 Batch 125 mg 50 mg 10 mg 125 mg 25 mg 50 mg n/a 60 mg 100 mg 20 mg 60 mg 50 mg 2 mg n/a n/a 50 mg 100 mg 250 mg 210 mg n/a 100 mg 100 mg 100 mg 150 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 43 4-methoxybenzene-1,3-dicarboxylic acid (2S)-2-[[[(2S)-5-oxopyrrolidin-2-yl]carbonyl]amino]pentanedioic acid 87.0% trans-phytomenadione, 12.6% cis-phytomenadione, 0.09% trans-epoxyphytomenadione; Vitamin K1 ; Batch 2 is valid until 28 February 2007 Norephedrin (4-butyl-4-hydroxy-1,2-diphenyl-3,5)-pyrazolidinedione Information Unit Sale Quantity Unit 40 mg 1 100 mg 1 0.05 mg 2 n/a 1 20 mg 1 1-methyl-4-phenylpiperidine (MPP) 50 mg 1 250 mg 1 Batch 1 is valid until 30 April 2007 250 mg 1 Batch 2 is valid until 30 April 2006 2 ml 1 250 mg 1 250 mg 1 99.0% CŒÿHŒŸKNœO—S 1619 0633 1036 1358 1358 1619 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C Leaflet Storage a a a a l a a a a a a l l i a a a l a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 90 f 79 l 79 a 79 a 79 a 79 j 79 a 79 a 79 a 79 +5°C a 79 +5°C a For extra charges please see 2.2 2019 0629,0904 See leaflet,1356 0420 0420 0421 1357 0189,0201,0630 0781 0148 0113,0114,0148, 0149 1138 0782,0796,1161 0422,1574 0422 1035 0632,1205 0632,1035 2042 0103 0683 1253,1988 0521 2301,2302 0522 0352 0286 0684 1036 Monograph 6 December 2006 1 1 2 1 1 2 E0800000 Plastic additive 04 P2155005 Plastic additive 05 P2155008 Plastic additive 08 P2155009 Plastic additive 09 P2155010 Plastic additive 10 P2155011 Plastic additive 11 © Council of Europe, all rights reserved 2006 1 P2155003 Plastic additive 03 1 1 1 1 1 1 n/a 3 1 1 1 2 1 1 1 2 3 1 1 1 Batch 1 Pilocarpine nitrate Pilocarpine nitrate for system suitability Pimobendan Pimobendan for system suitability Pimozide Pindolol Pipemidic acid trihydrate - reference spectrum Piperacillin Piperazine adipate Piperazine citrate Piperazine hydrate Piracetam Pirenzepine dihydrochloride monohydrate Piretanide Piretanide impurity A Piroxicam Piroxicam for system suitability Pivampicillin Pivmecillinam hydrochloride Pivmecillinam impurity C Reference Standard P2155001 Plastic additive 01 Order Code P1700000 Y0000106 Y0000525 Y0000401 P1750000 P1800000 Y0000061 P1890000 P1900000 P2000000 P2100000 Y0000288 Y0000038 P2120000 P2120002 P2130000 P2130100 P2150000 P2152000 P2152015 Catalogue No. 48-2006/4 500 mg 250 mg 250 mg 1 1 1 44 4,4',4''-[(2,4,6-trimethylbenzene-1,3,5-triyl)tris(methylene)]tris[2,6-bis(1,1-dimethylethyl)phenol] Synonym: 2,2',2'',6,6',6''-hexatert-butyl-4,4',4''-[2,4,6-trtimethyl-1,3,5benzenetriyl)trismethylene]triphenol Octadecyl 3-(3,5-di-tert-butyl-4-hydroxyphenyl)-propionate ; Batch 1 is valid until 31 August 2006 Information Unit Sale Quantity Unit 50 mg 1 20 mg 1 10 mg 1 0.1 mg 1 150 mg 1 100 mg 1 n/a 1 100 mg 1 94.5% Cœ–HœŸN—OŸS 250 mg 1 250 mg 1 250 mg 1 120 mg 1 99.8% CÿHŒÕNœOœ ; Batch 1 is valid until 31 March 2006 250 mg 1 100 mg 1 20 mg 1 4-phenoxy-3(1H-pyrrol-1-yl)-5-sulphamoylbenzoic acid 100 mg 1 10 mg 1 Batch 2 is valid until 31 March 2007 50 mg 1 99,2% CœœHœ„N–OÿS 100 mg 1 99.0% CœŒH–÷ClN–O—S 10 mg 1 methylene 2,2-dimethylpropanoate (2RS,4S)-2-[[[(hexahydo1H-azepin-1-yl)methylene]amino]methyl]-5,5-dimethylthiazolidin -4-carboxylate 2 ml 1 (2RS)-2-ethylhexyl) benzene-1,2-dicarboxylate Synonym: di(2-ethylhexyl)phthalate 100 mg 1 N,N'-ethylenedialcanamide Synonym: N,N'-diacylethylenediamines 500 mg 1 Epoxidised soya oil 500 mg 1 Epoxidised linseed oil 500 mg 1 Ethylene bis [3,3-di(3-1,1-dimethylethyl-4-hydroxyphenyl) butyrate] R Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a a a 79 79 79 79 79 79 79 79 Extra Price charges 79 g 79 g 79 a 79 g 79 a 79 a 79 l 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a For extra charges please see 2.2 30103,30105,30106, 30107 30101 90001,30114 30103,30104,30105, 30106 30103,30105,30106, 30107 30103,30105,30106, 30107 90001,30114 90001,90002,30114 0104 0104,0633 2179 2179 1254 0634,0871,1789 1743 1168,1169 0423 0424 0425 1733 2001 1556 1556 0944 0944 0808,0852 1359 1359 Monograph 6 December 2006 1 1 1 1 1 1 1 1 1 1 3 1 1 1 1 1 n/a 4 P2155014 Plastic additive 14 P2155015 Plastic additive 15 Plastic additive 16 Plastic additive 17 Plastic additive 18 Plastic additive 20 E1260000 Plastic additive 21 P2155022 Plastic additive 22 P2155023 Plastic additive 23 P2160000 Poliomyelitis vaccine (inactivated) BRP P2161000 Poliomyelitis vaccine (oral) BRP Poloxamer 124 Poloxamer 188 Poloxamer 237 Poloxamer 338 Poloxamer 407 Polyacrylate - reference spectrum Polymyxin B sulphate Polymyxin B sulphate for microbiological assay Polysorbate 20 - reference spectrum Polysorbate 40 - reference spectrum Polysorbate 60 - reference spectrum Polysorbate 80 - reference spectrum Poly(vinyl chloride) Potassium clavulanate - reference spectrum P2155016 P2155017 P2155018 O0140000 P2163920 P2164009 P2164020 P2164021 P2164030 P2170000 P2400000 Y0000355 Y0000289 Y0000290 Y0000291 Y0000007 P2600000 P2649610 © Council of Europe, all rights reserved 2006 1 P2155013 Plastic additive 13 1 n/a n/a n/a n/a 1 n/a 2 Batch Order Reference Standard Code P2155012 Plastic additive 12 Catalogue No. 48-2006/4 25 mg n/a n/a n/a n/a 100 mg n/a 30 mg 100 mg 100 mg 100 mg 100 mg n/a 120 mg 1 ml 0.6 mg 200 mg 100 mg 100 mg 500 mg 500 mg 100 mg 100 mg 200 mg 500 mg 250 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 5 5 1 1 1 1 1 1 1 1 1 1 Monograph 45 67.4% polymyxin B1, 7.8% polymyxin, 2.6% polymyxin B3, 7.3% polymyxin B1-I 203360 IU per vial Yes +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C a l l l l a l a a a a a l a d d a a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 90 90 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 0426 1914 0427 0428 90001,90002,30114 1140 1464 1464 1464 1464 1464 0733 0203 -20°C -80°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage 30103,30105,30106, 30107 1,3,5-tris(3,5-di-1,1-dimethylethyl-4-hydroxybenzyl)-1H,3H,5H-1, 30103,30105,30106 3,5-triazine-2,4,6-trione 2,2'-Di(octadecycloxy)-5,5'-spirobi(1,3,2-dioxaphosphorinane) R 30103,30105,30106 Dioctadecyl disulphide 30103,30104,30105, 30106 Didodecyl 3,3'-thiodipropionate R 30103,30105,30106 Dioctadecyl 3,3'-thiodipropionate R 30103,30105,30106 30103 Oleamide R 30103,30105,30106, 30107 Erucamide R 30103,30107 Copolymer of dimethyl butanedioate and 30103 1-(2-hydroxyethyl)-2,2,6,6-tetramethylpiperidin-4-ol Synonyms: copolymer of dimethyl succinate and (4-hydroxy-2,2,6,6-tetramethylpiperidin-1-yl)ethanol di(isooctyl)2,2'-[(dioctylstannylene)bis(thio)]diacetate 30110,30111 containing about 27% of (tri(isooctyl)2,2',2''- [monooctylstannylidyne)tris(thio)] triacetate. Tin-content of 15.4% 430-95-285 Ph. Eur. D-Antigen Units per ml for types 1-2-3, 0214,2066,2065, Yes respectively 2328,2061,2067, 1934,2329,20720 log ŒÕ CCID50/ml for types 1,2,3 and total virus content: 6.99, See leaflet,0215 Yes 6.06, 6.83 and 7.20, respectively Information Unit Sale Quantity Unit 200 mg 1 Tris (2,4-di-1,1-dimethylethylphenyl) phosphite R 6 December 2006 © Council of Europe, all rights reserved 2006 Prednisolone acetate for peak identification Prednisolone hexanoate Prednisolone pivalate Prednisolone sodium phosphate Prednisone Pregnenolone isobutyrate Prekallikrein activator in albumin BRP Prilocaine Prilocaine hydrochloride Prilocaine impurity E Primaquine diphosphate Primidone Primidone for peak identification Probenecid Procainamide hydrochloride Procaine benzylpenicillin Procaine hydrochloride Prochlorperazine maleate 1 1 1 3 3 4 1 1 1 1 2 1 1 1 1 2 1 1 1 1 1 5 Y0000582 P2804000 P2805000 P2810000 P2900000 P2920000 Y0000263 P2939000 P2939060 P2939025 P2940000 P2950000 Y0000369 P3000000 P3050000 P3090000 P3100000 P3200000 Prazosin hydrochloride Prednicarbate Prednicarbate impurity F Prednisolone P2680000 P2698000 P2698060 P2700000 1 1 2 2 3 Pravastatin 1,1,3,3-tetramethylbutylamine Prazepam -* psy Praziquantel Praziquantel impurity A Y0000204 P2669000 P2670000 P2675000 1 1 2 1 n/a 2 Batch P2800000 Prednisolone acetate Potassium hydrogen aspartate hemihydrate Potassium sorbate Povidone Povidone (iodinated) Pravastatin sodium - reference spectrum Pravastatin impurity A Reference Standard Order Code Y0000315 P2650000 P2660000 Y0000466 Y0000215 Y0000223 Catalogue No. 48-2006/4 10 mg 10 mg 100 mg 150 mg 50 mg 100 mg 1 ml 150 mg 100 mg 25 mg 500 mg 150 mg 5 mg 100 mg 100 mg 250 mg 100 mg 100 mg 120 mg 50 mg 100 mg 10 mg 150 mg 50 mg 150 mg 10 mg 1 1 1 1 1 1 3 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 46 96.3% Cœ„H–‡N÷OÿS; 39.7% CŒ–HœÕNœOœ (procaine) 100% CŒœHŒ÷NœOœ (¢£)-N-(methylphenyl)-2-(propylamino)propanamide Batch 3 is valid until 28 February 2007 29 IU per vial 99.1% CœŸH–ÿO‡ 1,2-dihydroprednicarbate 99.8% CŒ„Hœ÷NœOœ (RS)-2-benzoyl-1,2,3,6,7,11b-hexahydro-4H-pyrazino[2,1-a] isoquinolin-4-one ; Batch 1 is valid until 28 February 2007 Information Unit Sale Quantity Unit 50 mg 1 100 mg 1 50 mg 1 10 mg 1 n/a 1 10 mg 1 (3R,5R)-3,5-dihydroxy-7-[(1S,2S,6R,8S,8aR)-6-hydroxy-2-methyl -8-[[(2S)-2-methylbutanoyl]oxy]-1,2,6,7,8,8a-hexahydronaphtha len-1-yl]heptanoic acid (6'-epipravastatin) ; Batch 1 is valid until 30 November 2006 30 mg 1 76.4% pravastatin Yes Yes Yes +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a b a a a a a a a a a a a a a a a a c j a a 79 79 79 79 79 79 79 79 79 79 79 90 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 l 79 c For extra charges please see 2.2 0856 1467 1467 0335,0353,0354, 0735 0734,0736,0933, 0975,1467 0734 1212 0734,0736 0549,0735,0810 0354 0993 See leaflet,20615 1362 1363 1362,1363 0635 0584 0584 0243 0567 0115 0050 0244,20303 2059 1466 0855 0855 2076 0618 0685 1142 2059 2059 Monograph 6 December 2006 Propanol - reference spectrum Propofol Propofol for peak identification Propofol impurity J Propranolol hydrochloride Propranolol hydrochloride for performance test Propylene glycol dilaurate Propylene glycol monolaurate Propyl gallate Propyl parahydroxybenzoate Propylthiouracil Propyphenazone Protirelin D-His-Protirelin Proxyphylline Pseudoephedrine hydrochloride - * Drug Precursor Pseudoisoeugenyl 2-methylbutyrate for peak identification Purpureaglucoside A Purpureaglucoside B Pyrantel embonate Pyrantel impurity A © Council of Europe, all rights reserved 2006 P4050000 Pyrazinamide P4099900 Pyridostigmine bromide Y0000278 Y0000016 Y0000017 Y0000018 P3500000 P3600000 Y0000318 Y0000319 New P3640000 P3650000 P3700000 P3750000 P3760000 P3760020 P3800000 P3850000 Y0000387 P3900000 P4000000 Y0000402 Y0000403 1 2 n/a 3 2 2 2 3 1 1 2 2 1 3 3 2 1 2 1 1 1 1 1 1 2 n/a 1 1 P3390000 P3400000 P3490000 Y0000455 Y0000456 Promazine hydrochloride Promethazine hydrochloride Propacetamol hydrochloride - reference spectrum Propafenone hydrochloride Propafenone impurity B 2 P3350000 Proline 1 1 n/a 2 Batch 2 Progesterone Progesterone impurity C Proguanil hydrochloride - reference spectrum Proguanil impurity C Reference Standard Y0000182 Proguanil impurity D Order Code P3300000 Y0000148 Y0000179 Y0000181 Catalogue No. 48-2006/4 30 mg 50 mg n/a 290 mg 0.1 ml 20 mg 30 mg 20 mg 100 mg 100 mg 50 mg 100 mg 100 mg 200 mg 5.03 mg 0.5 mg 100 mg 100 mg 100 mg 25 mg 25 mg 10 mg 20 mg 100 mg 50 mg n/a 10 mg 10 mg 60 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0785,0910,0911, 1049 0475,1365,20303 0524,20303 1366 2103 2103 2002 0429 0429 2002 2002 Monograph 47 0859 1255 Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a l a a a g g a a a a a a c c a i a a a a a a g l g g a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 l 79 a For extra charges please see 2.2 2036 99.9% CŒœHŒ‡O ; Batch 2 is valid until 31 October 2006 1558 1558 2,6-bis (1-methylethyl)-1,4-benzoquinone 1558 Batch 1 is valid until 30 April 2006 0568,0923 Batch 2 is valid until 30 September 2006 0568 2087 1915 Batch 1 is valid until 1 November 2006 1039 0431,0852,1263 0525 0636 5.03 mg per vial of pure protirelin peptide CŒÿHœœNÿO÷ 1144 approx. 0.1 mg per vial ; Batch 1 is valid until 30 September 2006 1144 0526 0487,1367 Anise oil 2108 0117 0117 1680 1-methyl-2-[(Z)-2-(thiophen-2-yl)ethenyl]-1,4,5,6-tetrahydropyri 1680 midine 1-[2-[(2RS)-2-hydroxy-3-(propylamino)propoxy]phenyl] -3-phenylpropenone Information Unit Sale Quantity Unit 250 mg 1 10 mg 1 (20R)-20-hydroxypregn-4-en-3-one n/a 1 10 mg 1 1,5-bis(4-chlorophenyl)biguanide ; Batch 1 is valid until 31 December 2005 10 mg 1 1,5-bis(1-methylethyl)biguanide ; Batch 1 is valid until 30 November 2006 6 December 2006 2 2 1 1 1 1 3 2 5 1 R0150000 Ranitidine hydrochloride Y0000416 Ranitidine impurity J Ranitidine for system suitability Repaglinide Repaglinide for system suitability Repaglinide impurity E Y0000411 Y0000457 Y0000458 Y0000459 R0200000 Reserpine R0250000 Residual solvents solution class 1 R0300000 Retinol acetate R0290000 Retinol esters 1 1 1 3 1 1 2 R0145020 Ramipril impurity D R0500500 Reviparin sodium Y0000377 Ribavirin Y0000353 Ribavirin for system suitability R0600000 Riboflavin R0630000 Riboflavin sodium phosphate Y0000149 Rifabutin © Council of Europe, all rights reserved 2006 2 R0145015 Ramipril impurity C 1 1 1 1 1 2 4 2 2 Batch 2 Pyridostigmine impurity A Pyridoxine hydrochloride Pyrimethamine Pyrrolidone Quinidine sulphate Quinine sulphate Rabies vaccine (inactivated) for veterinary use BRP Ramipril Ramipril impurity A Reference Standard R0145010 Ramipril impurity B Order Code P4099910 P4100000 P4200000 Y0000659 Q0100000 Q0200000 R0100000 R0145000 R0145005 Catalogue No. 48-2006/4 250 mg 100 mg 1 mg 100 mg 250 mg 150 mg 100 mg 100 mg 1500 mg 1000 mg 100 mg 0.00025 mg 20 mg 20 mg 6 mg 5 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1368 1368 1255 0245 0288 2180 0017,0018,0019 0017,0018,0019 See leaflet,0451 1368 1368 Monograph 0946 2135 2135 2-ethoxy-4-[2-[[(1R)-3-methyl-1-[2-(piperidin-1-yl)phenyl]butyl] 2135 amino]-2-oxoethyl]benzoic acid 99.8% C––H÷ÕNœO„ 0528 Batch 1 is valid until 31 May 2006 20424 1044000 IU per g 0218,0219,0220, 1192,1193 0217,0218,0219, 0220 0828 100.0% C‡HŒœN÷O— 2109 2109 Vitamin B2 ; Batch 2 is valid until 31 October 2006 0292,0786 0786 96.3% C÷—HÿœN÷OŒŒ 1657 48 For extra ethyl (2S)-2-[(3S,5aS,8aS,9aS)-3-methyl-1,4-dioxodecahydro 1368 -1H- cyclopenta[e]pyrrolo[1,2a]pyrazin-2-yl]-4-phenylbutanoate (ramipril diketopiperazine) ; Batch 1 is valid until 31 May 2006 Batch 1 is valid until 30 April 2006 0946,1453 1,1'-N-[methylenebis(sulphanediylethylene)]bis(N'-methyl-2-nitro 0946 ethene-1,1-diamine) Information Unit Sale Quantity Unit 20 mg 1 pyridin-3-yl-dimethylcarbamate 100 mg 1 250 mg 1 20 mg 1 300 mg 1 300 mg 1 86 mg 3 11 IU per vial 20 mg 1 10 mg 1 (2S,3aS,6aS)-1-[(S)-2-[[(S)-1-(methoxycarbonyl)-3phenylpropyl]amino]propanoyl]octahydrocyclopenta[b]pyrrole-2 -carboxylic acid (ramipril methylester) 10 mg 1 (2S,3aS,6aS)-1-[(S)-2-[[(S)-1-[(methylethoxy)carbonyl]-3phenylpropyl]amino]propanoyl]octahydrocyclopenta[b]pyrrole2-carboxylic acid (ramipril isopropyl ester) 10 mg 1 (2S,3aS,6aS)-1-[(S)-2-[[(S)-1-(ethoxycarbonyl)-3-cyclohexylprop yl]amino]propanoyl]octahydrocyclopenta[b]pyrrole-2- carboxylic acid (hexahydroramipril) ; Batch 1 is valid until 31 December 2005 +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C a a g c a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 90 c 79 a 79 a +5°C a +5°C a +5°C a +5°C a +5°C a +5°C a charges please see 2.2 Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C Leaflet Storage 6 December 2006 1 3 2 2 2 2 1 1 1 Rutoside trihydrate Saccharin Saccharin sodium Salbutamol Salbutamol impurity B Y0000105 S0040000 S0050000 S0100000 Y0000030 Y0000071 Salbutamol impurity D Y0000031 Salbutamol impurity F Y0000034 Salbutamol impurity G Y0000032 Salbutamol impurity I S0150000 S0200000 Y0000405 Y0000422 Y0000423 © Council of Europe, all rights reserved 2006 Salbutamol sulphate Salicylic acid Salicylic acid impurity B Salmeterol xinafoate Salmeterol for system suitability 1 1 1 2 2 Rocuronium for peak identification Rocuronium bromide - reference spectrum Roxithromycin Roxithromycin for system suitability Rubella vaccine (live) BRP Ruscogenins 1 n/a 4 1 1 1 1 1 3 1 1 3 n/a 1 1 1 1 Y0000527 Y0000594 R1500000 Y0000220 R2000000 Y0000494 Batch Rifabutin impurity A Rifampicin Rifampicin quinone Rifamycin B Rifamycin S Rifamycin sodium Rilmenidine dihydrogenophosphate - reference spectrum Rilmenidine for system suitability Risperidone Risperidone for system suitability RK 13 cells Reference Standard Order Code Y0000184 R0700000 R0800000 R0900000 R0950000 R1000000 Y0000250 Y0000187 R1000600 Y0000370 R1300000 Catalogue No. 48-2006/4 50 mg 100 mg 10 mg 40 mg 25 mg 0.006 mg 5 mg 5 mg 10 mg 100 mg 30 mg 50 mg 50 mg 5 mg 10 mg n/a 125 mg 5 mg 18 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 5 1 49 4-hydroxyisophthalic acid 99.6% C–ÿH÷—NOŸ (1RS)-2-[(1,1-dimethylethyl)amino]-1-(4-hydroxyphenyl)ethanol (1RS)-2-[(1,1-dimethylethyl)amino]-1-hydroxyethyl]-2-hydroxybenzaldehyde 1,1'-[oxybis[methylene(4-hydroxy-1,3-phenylene)]]bis[2-[(1,1dimethylethyl)amino]ethanol] 91.3% salbutamol impurity G; 2-[benzyl(1,1-dimethylethyl)amino]-1-[4-hydroxy-3-(hydroxymethyl)phenyl]ethanone (1RS)-2-[(1,1-dimethylethyl)amino]-1-[3-(hydroxymethyl)-4benzyloxyphenyl]ethanol 3.6 logŒÕ (ie 4000) infective viral units per vial 38.2% ruscogenin 60.4% neoruscogenin 96.8% C÷ŒHŸÿNœOŒ— Information Unit Sale Quantity Unit 20 mg 1 (N-(2-methylpropyl)-4-piperidone) 500 mg 1 100 mg 1 50 mg 1 50 mg 1 300 mg 1 856 IU per mg n/a 1 30 mg 1 100 mg 1 20 mg 1 1 ml 2 cell lines (kidney, rabbit) titration of live measles, mumps and rubella vaccines Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -80°C +5°C -20°C +5°C +5°C +5°C -180°C +5°C +5°C +5°C +5°C +5°C -20°C Leaflet Storage a a a a a a a a a a a a a a g l a a d a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 90 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 c 79 l 79 a 79 g 79 g 100 d For extra charges please see 2.2 0687 0366,1156 0366 1765 1765 0529,0687 0529,0687 0529,0687 0529,0687 1795 0947 0787 0529,1033 0529,0687 1764 1764 1146 1146 1057,0162 1847 1657 0052 0052 0432 0432 0432,20702 2020 2020 1559 1559 0162,1057 Monograph 6 December 2006 © Council of Europe, all rights reserved 2006 New Y0000711 Somatropin/desamidosomatropin resolution mixture S0950000 Sorbic acid S0930000 Sodium valproate S0945000 Somatostatin S0947000 Somatropin 1 1 3 2 2 1 1 1 1 1 3 1 2 1 n/a 1 1 1 2 2 2 n/a 2 1 1 n/a n/a 1 1 1 1 2 S0450000 S0460000 Y0000371 S0500000 S0600000 S0650000 S0660000 Y0000014 S0695000 Y0000300 Y0000039 S0700000 S0710000 S0750000 S0760000 S0765000 S0781000 S0780000 Y0000620 S0785000 Y0000210 Y0000268 S0800000 Y0000662 S0808000 S0808060 S0900000 Serine Sertaconazole nitrate Sestamibi labelling kit Silicone elastomer Silicone oil Simvastatin Sisomicin sulphate Sodium alendronate Sodium amidotrizoate Sodium aminosalicylate dihydrate - reference spectrum Sodium ascorbate Sodium calcium edetate Sodium cetostearylsulphate Sodium cromoglicate Sodium cyclamate Sodium diclofenac Sodium hyaluronate - reference spectrum Sodium hyaluronate BRP Sodium laurilsulfate Sodium picosulphate Sodium polystyrene sulphonate - reference spectrum Sodium propionate - reference spectrum Sodium salicylate Ribonucleic acid Sodium stearyl fumarate Sodium stearyl maleate Sodium taurocholate BRP 1 1 1 Batch Order Reference Standard Code S0360000 Selegiline hydrochloride S0360090 (RS)-Selegiline hydrochloride S0400000 Senna extract Catalogue No. 48-2006/4 33 mg 100 mg 50 mg 125 mg 1 uc 2000 mg 1 ml 100 mg 50 mg 150 mg 125 mg n/a 50 mg 100 mg 100 mg 10 mg 100 mg 100 mg n/a 300 mg 40 mg 100 mg n/a n/a 100 mg 100 mg 50 mg 10 mg 10000 mg 150 mg 2.55 mg 35 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Unit Sale Quantity Unit 50 mg 1 25 mg 1 50 mg 1 50 2.55 mg somatostatin peptide per vial 1.69 mg somatropin monomer per vial ; Batch 1 is valid until 31 October 2006 1.7 mg somatropin per vial Batch 1 is valid until 31 March 2006 100.0 % 99.4% Cœ—H–‡O— ; Batch 2 is valid until 30 September 2006 83.4% C–‡H‡÷NŒÕO–÷S— 83.4% C÷HŒœNNaOŸPœ Information Yes Yes -20°C +5°C +5°C +5°C +5°C +5°C Room temp. +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a c a a a a a a c a a a l a a a a a a l a a a l l a a a a a 79 150 150 90 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a For extra charges please see 2.2 0678 0949 See leaflet,0950, 0951,0952 0950,0951,0952 0592 1260 1260 0206,0207,0208, 1261 0788,1027 1148 1926 30109 30108 1538,1563 1351 1564 1150 1993 1791 0231 0847 0562 0774 1002,1281 1472 0912 0802 1031 1909 2041 0413 2090 1567 1567 0350 Monograph 6 December 2006 n/a 1 1 n/a n/a 1 1 1 1 S1400000 Streptomycin sulphate S1500000 Succinylsulfathiazole S1600000 Sucrose S1608100 S1609000 Y0000529 Y0000528 Y0000550 S1700000 © Council of Europe, all rights reserved 2006 Sufentanil - reference spectrum Sufentanil citrate - reference spectrum Sulbactam sodium Sulbactam Sulbactam for peak identification Sulfacetamide sodium 1 S1350000 Stearyl alcohol 1 1 1 1 1 1 3 1 1 2 Spirapril hydrochloride monohydrate Spirapril for system suitability Spironolactone Squalane Stanozolol Stanozolol impurity A Starch BRP Y0000381 Y0000332 S1200000 Y0000185 S1250000 S1250010 S1300000 2 1 1 4 Y0000408 Stavudine Y0000421 Stavudine for system suitability S1340000 Stearic acid Spectinomycin hydrochloride Spectinomycin for system suitability Spectinomycin sulphate tetrahydrate Spiramycin Y0000597 Y0000549 New Y0000655 S1100000 1 1 Y0000114 Sotalol hydrochloride Y0000115 Sotalol impurity B Batch 1 3 Reference Standard Order Code Y0000385 1,4-Sorbitan S1000000 Sorbitol Catalogue No. 48-2006/4 n/a n/a 10 mg 150 mg 20 mg 50 mg 100 mg 100 mg 100 mg 250 mg 60 mg 15 mg 100 mg 0.25 ml 125 mg 10 mg 50000 mg 100 mg 10 mg 100 mg 100 mg 20 mg 10 mg 200 mg 25 mg 20 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 Monograph 51 99.7% C‡HŒŒNO—S 78 500 IU per ampoule; International standard provided for an interim period 100% CŒ‡H–‡O Plastic additive 19 99.6% CŒÕHŒœNœO÷ (5¶,17ß)-17-hydroxy-17-methylandrostan-3-one Batch 2 is valid until 30 September 2006 99.7% C–ÕHÿœ 4530 IU per mg Spiramycin I: 87.9%, Spiramycin II: 0.2%, Spiramycin III: 5.3% 95.9% CœœH–ŒClNœO—Sœ Yes Yes l l a b a a a a a a a a a a a a a a a a a a c a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a For extra charges please see 2.2 +5°C -20°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C Leaflet Storage 2130 2130 Yes 0229,0882,2058, 30103,30105,30106, 30107 0702,0753,0801, 0802,0847,0969, 1123,1340,1411 0032,0033,0053, 0485,20702 0357 0177,0178,0187, 0188,0204,0209, 1061,1570 1569 1269 2209 2209 2209 Yes 0107 1152 1658 0179,0293,1982, 1983,20702 1766 1766 0688 1630 1568 1568 0350 2048 0435,0436,0437, 1235,1236,1337, 1381,1531,2048 2004 N-[4-[[(1-methylethyl)amino]acetyl]phenyl]methanesulphonami- 2004 de 81.3% CŒ÷HœÿClœNœOŸ and CŒ÷Hœ‡ClœNœOŸ 1152 Information Unit Sale Quantity Unit 50 mg 1 99.2% CÿHŒœO— 1200 mg 1 97.9 % CÿHŒ÷Oÿ ; Batch 2 is valid until 28 February 2007 6 December 2006 2 1 1 1 © Council of Europe, all rights reserved 2006 Sumatriptan for system suitability Suxamethonium chloride Suxibuzone Suxibuzone impurity B Y0000027 S2200000 S2400000 S2400004 1 1 2 3 1 2 2 2 1 1 1 1 1 2 3 Sulfathiazole Sulfinpyrazone Sulfinpyrazone impurity A Sulfinpyrazone impurity B Sulfisomidine Sulindac Sulpiride Sulpiride impurity A Sulpiride impurity B Sultamicillin Sultamicillin tosilate Sultamicillin for peak identification Sumatriptan succinate Sumatriptan impurity C S2158000 S2159000 S2159010 S2159015 S2160000 S2180000 S2190000 S2191000 S2192000 Y0000530 Y0000531 Y0000532 Y0000022 Y0000025 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 Batch Y0000026 Sumatriptan impurity mixture Sulfadiazine Sulfadimidine Sulfadoxine Sulfafurazole Sulfaguanidine Sulfamerazine Sulfamethizole Sulfamethoxazole Sulfamethoxazole impurity A Sulfamethoxazole impurity F Sulfamethoxypyridazine Sulfanilamide Sulfapyridine Sulfasalazine Sulfasalazine derivative for resolution Reference Standard Order Code S1800000 S1900000 S1950000 S1975000 S1975600 S2000000 S2050000 S2100000 Y0000412 Y0000413 S2150000 S2151000 S2159100 S2155000 S2155010 Catalogue No. 48-2006/4 2 mg 1000 mg 50 mg 10 mg 3 mg 100 mg 30 mg 20 mg 20 mg 50 mg 50 mg 100 mg 20 mg 30 mg 10 mg 200 mg 10 mg 50 mg 5 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0294 0295 0740 0741 1476 0358,1571 0637 0108 0108 0108 0638 1571 0863 0863,1457 0863 Monograph 52 (4-butyl-3,5-dioxo-1,2-diphenylpyrazolidin-4-yl)methyl ethyl butanedioate 1573 0248 1574 1574 Yes Yes Yes -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage c a a a c a a a a a a a a a a a a c c 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 g 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a For extra charges please see 2.2 0742 0790 1,2-diphenyl-4-[2-(phenylsulphonyl)ethyl)pyrazolidine-3,5-dione 0790 1,2-diphenyl-4-(2-phenylthioethyl)pyrazolidine-3,5-dione 0790 0639 Contains 0.3% m/m of E-isomer 0864 1045,1348 2-aminomethyl-1-ethylpyrrolidine 1045 methyl 5-sulphamoyl-2-methoxybenzoate 1045 2211 68.5% Cœ—H–ÕN÷O„Sœ 2212 2211 98.8% CŒ‡HœŸN–OÿS 1573 [3-[2-(dimethylamino)ethyl]-1-(hydroxymethyl)-1Hindol-5-yl]-N- 1573 methylmethanesulphonamide Batch 2 is valid until 31 December 2006 1573 Batch 1 is valid until 30 June 2006 Information Unit Sale Quantity Unit 100 mg 1 100 mg 1 100 mg 1 100 mg 1 60 mg 1 100 mg 1 100 mg 1 50 mg 1 5 mg 1 N-(4-(5-methyl)-isoxazol-3-ylsulphamoyl)phenylacetamide 5 mg 1 4-amino-N-(3-methylisoxazol-5-yl)benznesulphonamide 50 mg 1 100 mg 1 20 mg 1 250 mg 2 99.9 % CŒ‡HŒ÷N÷O—S 20 mg 1 2-hydroxy-5-[[4-[[(6-methylpyridin-2-yl)amino]-sulfonyl]phenyl] azo]benzoic acid 6 December 2006 1 1 1 1 1 1 1 1 1 1 1 1 1 1 3 T0040000 Temazepam - * psy Y0000344 Temazepam impurity C Y0000345 Temazepam impurity D Y0000346 Temazepam impurity F Y0000347 Temazepam impurity G T0040800 Y0000621 Y0000666 Y0000622 Y0000665 Y0000623 Y0000624 Y0000535 T0050000 T0050015 1 T0100000 Testosterone © Council of Europe, all rights reserved 2006 1 1 1 T0060000 Terconazole T0071000 Terfenadine T0080000 Terfenadine impurity A Tenoxicam Terazosin hydrochloride dihydrate Terazosin for system suitability Terazosin impurity A Terazosin impurity E Terazosin impurity L Terazosin impurity N Terbinafine hydrochloride Terbutaline sulphate Terbutaline impurity C 1 New Y0000652 Tamsulosin impurity H New New New New New New 50 mg 80 mg 50 mg 10 mg 10 mg 10 mg 1 1 2 1 1 1 250 mg 250 mg 100 mg 30 mg 100 mg 40 mg 0.5 mg 10 mg 10 mg 10 mg 10 mg 10 mg 100 mg 15 mg 5 mg 5 mg 5 mg 50 mg 5 mg 10 mg 1 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 See leaflet,0064 See leaflet,0064 1574 Monograph 0954 0954 0954 0879 0954 53 1-[4-(1,1-dimethylethyl)phenyl]-4-[4-(hydroxydiphenylmethyl) piperidin-1-yl]butan-1-one (ketone) Yes Yes Yes Yes Yes Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage g a a a a a a a a a a a a g a a a j a a a g a a A a f f 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 90 90 Extra Price charges 79 a 6 December 2006 For extra charges please see 2.2 0410,1373 1270 0955 0955 1156 2021 2021 2-chloro-6,7-dimethoxyquinazolin-4-amine 2021 2,2'-(piperazine-1,4-diyl)bis(6,7-dimethoxyquinazolin-4-amine) 2021 1-(furan-2-ylcarbonyl)piperazine 2021 1-[[(2RS)-tetrahydrofuran-2-yl]carbonyl]piperazine 2021 1734 0690 1-(3,5-dihydroxyphenyl)-2-[(1,1-dimethylethyl)amino]-ethanone 0690 ; Batch 2 is valid until 30 April 2006 (3RS)-7-chloro-1-methyl-2-oxo-5-phenyl-2,3-dihydro-1H-1,4benzodiazepin-3-yl acetate (3RS)-7-chloro-3-methoxy-1-methyl-5-phenyl-1,3-dihydro-2H1,4-benzodiazepin-2-one (5RS)-7-chloro-1-methyl-5-phenyl-4,5-dihydro-1H-1,4benzodiazepine-2,3-dione (5RS)-7-chloro-1,4-methyl-5-phenyl-4,5-dihydro-1H-1,4benzodiazepine-2,3-dione 0808,0852 1046 1046 2131 2131 (2R)-N-[2-(2-ethoxyphenoxy)ethyl]-1-(4-methoxyphenyl)propan- 2131 2-amine (2R)-N-[2-(2-ethoxyphenoxy)ethyl]-1-(4-methoxyphenyl)propan- 2131 2-amine 2.6 x10Ï Cfu per vial Information Unit Sale Quantity Unit 10 mg 1 4-butyl-4-(hydroxymethyl)-1,2-diphenyl-1,2-dihydro-4Hpyrazole-3,5-dione 1 mg 1 6.5 x10Ì Cfu per vial 1 1 1 Batch S5000001 Swine erysipelas bacteria, serotyp 1 (for vaccines - vet. use) BRP S5000002 Swine erysipelas bacteria, serotyp 2 (for vaccines - vet. use) BRP T0010000 Talampicillin hydrochloride T0014000 Tamoxifen citrate T0015000 Tamoxifen citrate for performance test New Y0000650 Tamsulosin hydrochloride New Y0000653 Tamsulosin racemate New Y0000651 Tamsulosin impurity D Order Reference Standard Code S2400006 Suxibuzone impurity C Catalogue No. 48-2006/4 1 1 1 n/a 1 1 1 2 1 Tetryzoline hydrochloride Theobromine Theophylline Theophylline - reference spectrum Thiamazol Thiamazol impurity A Thiamazol impurity C Thiamine hydrochloride Thiamine impurity E Thiamine nitrate - reference spectrum Thiamphenicol Thioctic acid Thioctic acid for system suitability Thioctic acid containing impurity B Thiomersal Thiopental Thioridazine - reference spectrum Thioridazine hydrochloride Y0000460 T0700000 T0800000 Y0000294 Y0000336 Y0000372 Y0000373 Y0000467 Y0000059 Y0000060 T1100000 Y0000546 Y0000592 Y0000545 Y0000109 T1200000 Y0000150 T1300000 © Council of Europe, all rights reserved 2006 n/a 1 Y0000015 Tetrazepam - reference spectrum Y0000008 Tetrazepam impurity C n/a 1 1 1 1 1 1 n/a 1 100 mg 0.365 mg 100 mg 1 2 2 n/a 125 mg 110 mg 10 mg 30 mg 30 mg 500 mg n/a 50 mg 10 mg 100 mg 100 mg n/a 125 mg 10 mg 20 mg 10 mg 10 mg n/a 20 mg n/a n/a 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 2 1 1 0057 0644 0173,0198,0199, 0210,0211,1654 1738 1738 1325 0297 1048 1048 1048 1373 1373 1048 1048 0297 See leaflet,20708 Monograph 54 99.8% C‡HŒ÷OœSœ Yes +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C -20°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C Leaflet Storage l a a a a a a l g a a a l a a a a a l a g c a l 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 c 79 a 79 a 79 a 79 a 79 l 90 c 6 December 2006 For extra charges please see 2.2 0531 0109 1648 1648 1648 1625 0212 2005 0586,20303 2101 0298 0300,0301 0299,0302 1706 1706 1706 0303 3-[(4-amino-2-methylpyrimidin-5-yl)methyl]-5-(2-hydroxyethyl)- 0303,0531 4-methyl-4-thiazolidine-2-thione 7-chloro-5-cyclohexyl-1-methyl-1,3-dihydro-2H-1,4-benzodiazepin-2-one 365 μg per vial of pure tetracosactide peptide CŒ–ÿHœŒÕN÷ÕO–ŒS 96.7% CœœHœ—ClNœO‡ ; Batch 1 is valid until 31 March 2006 Information Unit Sale Quantity Unit 10 mg 1 50 mg 1 25 mg 1 100 mg 1 15 mg 1 15 mg 1 25 mg 1 250 mg 1 n/a 1 11 mg 1 469 IU per ampoule for assays in guinea pig 496 IU per ampoule for assays in mice T0499000 1,3,4,6-Tetra-O-acetyl-2-O-trifluoromethane-sulphonyl-ß - ref spectrum T0500000 Tetracaine hydrochloride T0550000 Tetracosactide T0600000 Tetracycline hydrochloride Batch 2 1 1 1 1 1 1 1 n/a 2 Reference Standard Testosterone acetate Testosterone caproate Testosterone decanoate Testosterone enantate Testosterone for impurity D identification Testosterone for system suitability Testosterone isocaproate Testosterone propionate Testosterone propionate - reference spectrum Tetanus vaccine (adsorbed) BRP Order Code T0200000 T0210000 T0240000 T0250000 Y0000342 Y0000343 T0260000 T0300000 Y0000170 T0400000 Catalogue No. 48-2006/4 Thioridazine for system suitability Thioxanthene Thioxanthone Threonine Thymol Tiabendazole Tiamulin for peak identification Tiamulin hydrogen fumarate Tiamulin - reference spectrum Tianeptine sodium - reference spectrum Tianeptine for system suitability Tianeptine impurity A Tiapride hydrochloride Tiapride N-oxide Tiaprofenic acid Tiaprofenic acid impurity C Tibolone - reference spectrum Tibolone for system suitability Ticarcillin monosodium Reference Standard T1423000 Ticlopidine hydrochloride T1423025 Ticlopidine impurity F Y0000325 Tilidine hydrochloride hemihydrate - reference spectrum T1450000 Timolol maleate Y0000644 (R)-timolol T1470000 Tinidazole T1471000 Tinidazole impurity B T1490000 Tinzaparin sodium Y0000292 Tioconazole - reference spectrum Y0000282 Tioconazole for system suitability T1500000 Tobramycin Y0000383 All-rac-alpha-tocopherol for peak identification Y0000384 All-rac-alpha-tocopheryl acetate for peak identification T1550000 alpha-Tocopherol T1600000 alpha-Tocopheryl acetate © Council of Europe, all rights reserved 2006 T1420010 Ticarcillin impurity A Order Code Y0000541 T1305100 T1305000 T1340000 T1350000 T1410000 Y0000414 Y0000333 Y0000379 Y0000151 Y0000152 Y0000153 T1405000 T1405050 T1410900 T1410910 New Y0000748 New Y0000668 Y0000465 Catalogue No. 48-2006/4 3 2 n/a 2 1 1 3 1 n/a 1 2 1 1 5 6 1 1 2 2 1 1 1 1 1 n/a n/a 1 1 1 1 1 1 n/a 1 1 Batch 50 mg 10 mg n/a 50 mg 20 mg 100 mg 20 mg 250 mg n/a 50 mg 250 mg 15 mg 15 mg 250 mg 250 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 97.7% Cœ„H—ÕOœ; Vitamin E 98.9% C–ŒH—œO– 55 91.6% CŒ‡H–ŸN—O„ 1-(2-ethylsulphonylethyl)-2-methyl-4-nitroimidazole 6-(2-chlorobenzyl)-4,5,6,7-tetrahydrothieno[3,2-c]pyridine Information Unit Sale Quantity Unit 0.21 mg 1 20 mg 1 10 mg 1 50 mg 1 50 mg 1 50 mg 1 10 mg 1 450 mg 1 99.1% C–œH—ŒNO‡S n/a 1 n/a 1 30 mg 1 20 mg 1 ethyl 7-bromoheptanoate 60 mg 1 20 mg 1 50 mg 1 20 mg 1 (¢£)-2-(5-benzoyl-3-thienyl)propanoic acid n/a 1 10 mg 1 250 mg 1 93.2% CŒ—HŒ—NœNaOÿSœ Correction factor 1.054 50 mg 1 89.8%; (2S,5R,6R)-3,3-dimethyl-7-oxo-6-[[(thiophen-3-yl)acetyl]amino]-4-thia-1-azabicyclo[3.2.0]heptane-2-carboxylic acid (decarboxyticarcillin) 1050 1050 1767 0572 0572 1051 1051 0828 2074 2074 0645 0692 0439 0692,1256,20432 0439,0691,1257 For extra 0956 0586 1347 1347 0785,1049 0791 0866 1659 1659,1660 1660 2022 0505 2022 1575 1575 1157 1157 1739 1739 0956 Monograph +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 g 79 g 79 l 79 l 79 a 79 a 79 a 79 a 79 a 79 a 79 l 79 b 79 a a a l +5°C g Yes +5°C g +5°C a +5°C a +5°C a l Yes +5°C a +5°C a Yes +5°C a Yes +5°C a +5°C a +5°C a charges please see 2.2 Yes Yes Yes Leaflet Storage 6 December 2006 T1975000 Triazolam - * psy Y0000165 Tribenoside Y0000166 Tribenoside impurity A Y0000330 Tributyl acetylcitrate - reference spectrum © Council of Europe, all rights reserved 2006 1 1 2 n/a 3 2 1 1 1 1 n/a n/a 1 3 1 1 T1810000 T1810030 T1820000 T1820002 T1820004 T1850000 T1899000 G0400010 T1899990 T1900000 T1950000 Y0000050 Tranexamic acid Tranexamic acid impurity C Trapidil Trapidil impurity A Trapidil impurity B Tretinoin 3,4,6-Tri-O-acetyl-D-glucal - reference spectrum Triacetin - reference spectrum Triamcinolone Triamcinolone acetonide Triamcinolone hexacetonide Triamcinolone impurity C 1 Y0000496 Trandolapril impurity D 2 1 1 1 1 1 Tramadol impurity E Tramazoline hydrochloride monohydrate Tramazoline impurity A Tramazoline impurity B Y0000157 Y0000072 Y0000065 Y0000066 1 1 1 1 1 1 2 2 Batch Y0000501 Trandolapril Y0000495 Trandolapril impurity C RRR-alpha-Tocopheryl hydrogen succinate Tolbutamide Tolfenamic acid Tolnaftate Torasemide anhydrous Torasemide for system suitability Tramadol hydrochloride Tramadol impurity A Reference Standard Order Code T1610000 T1700000 Y0000154 T1707000 Y0000461 Y0000462 Y0000155 Y0000156 Catalogue No. 48-2006/4 10 mg 150 mg 30 mg n/a 50 mg 10 mg 50 mg 20 mg 20 mg 100 mg n/a n/a 150 mg 100 mg 100 mg 10 mg 10 mg 10 mg 10 mg 20 mg 10 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1681 1597 1597 1597 1258,1259 0304 2039 1158 2132 2132 1681 1681 Monograph 1065 98.9% Cœ„H–÷Oÿ 1740 3,5,6-tri-O-benzyl-1,2-O-(1-methylethylidene)-¶-D-glucofuranose 1740 1770 56 9-fluoro-11ß-16alpha,17,21-tetrahydroxypregn-4-ene-3,20dione (pretriamcinolone) 5-methyl-[1,2,4]triazolo[1,5-a]pyrimidin-7-ol 1,2,4-triazol-3-amine (4-(aminomethyl) cyclohex-1-enecarboxylic acid) Yes +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a a a l l a a a a a a a a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 a 79 a 79 a 79 a 79 a 79 a 79 a j a c l For extra charges please see 2.2 0875 0875 1576 1576 1576 0693,1019,1385 1325 1106 1376 0533,0867,1075 0533,0867 1376 2245 (2S,3aR,7aS)-1-[(2S)-2-[[(1S)-3-cyclohexyl-1-(ethoxycarbonyl)pr 2245 opyl]amino]propanoyl]octahydro-1H-indole-2-carboxylic acid (hexahydrotrandolapril) ethyl (2S)-2-[(3S,5aS,9aR,10aS)-3-methyl-1,4-dioxodecahydro 2245 pyrazino[1,2-a]indol-2(1H)-yl]-4-phenylbutanoate (trandolapril diketopiperazine) N-(naphthalen-1-yl)-4,5-dihydro-1H-imidazol-2-amine 75% CŒ—HŒ„N–ÕO; mixture of 1-acetyl-2-[(5,6,7,8-tetrahydronaphthalen-1-yl) amino]-4,5- dihydro-1H-imidazole and N-(4,5-dihydro-1H-imidazol-2-yl)-N-(5,6,7,8- tetrahydronaphthalen-1-yl)acetamide Information Unit Sale Quantity Unit 125 mg 1 98.6% C––H—÷O— 100 mg 1 100 mg 1 60 mg 1 10 mg 1 0.4 mg 1 75 mg 1 15 mg 1 (1RS,2SR)-2-[(dimethylamino)methyl]-1-(3-methoxyphenyl)cyclohexanol 10 mg 1 (2RS)-2-[(dimethylamino)methyl]cyclohexanone 6 December 2006 Trimethoprim impurity B Trimethoprim impurity E Trimethyltetradecylammonium bromide Trimipramine maleate Trimyristin Tristearin Trolamine Trometamol Tropicamide Tropisetron hydrochloride Tropisetron impurity B Tropine Trospium chloride Trospium impurity A Trospium impurity B Trospium impurity C T2200010 T2200025 New T2450000 T2500000 T2500100 T2501200 T2545000 T2550000 T2580000 Y0000616 Y0000618 T2580300 Y0000429 Y0000432 Y0000431 Y0000430 © Council of Europe, all rights reserved 2006 Y0000497 Troxerutin Trihexyphenidyl hydrochloride Trihexyphenidyl impurity A Trilaurin Trimetazidine dihydrochloride - reference spectrum Trimetazidine for system suitability Trimethadione Trimethoprim Trimethoprim for system suitability Tri-n-butyl phosphate Tricaprin Tricaproin Tricaprylin Trichloroacetic acid - reference spectrum Trichlorotrifluoroethane Triethyl citrate - reference spectrum Trifluoperazine hydrochloride Triflusal Triflusal impurity B Reference Standard Y0000108 Y0000068 T2009000 Y0000092 Y0000093 T2100000 T2200000 New Y0000684 Order Code Y0000279 T1977990 T1977995 T1978000 Y0000111 T1985000 T1986000 T2000000 T2005000 T2005010 Catalogue No. 48-2006/4 1 3 2 2 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 n/a 1 1 1 1 1 1 1 1 n/a 1 n/a 1 1 1 Batch 30 mg 100 mg 20 mg 1250 mg n/a 50 mg 250 mg 50 mg 0.00075 mg 10 mg 20 mg 200 mg 100 mg 500 mg 100 mg 1000 mg 100 mg 50 mg 40 mg 10 mg 50 mg 10 mg 20 mg 15 mg 5 mg 1 1 1 1 1 1 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1626 1626 1410 1741 1741 0440 0060 0060 1682 1410 1410 1410 1967 0393 1479 0059,20303 1377 1377 Monograph 57 2133 Yes +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C -20°C Leaflet Storage a a a a g c c a a a g a a g a g g a a c l a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 79 c 79 c 79 c 79 l 79 a 79 l 79 a 79 a 79 a For extra charges please see 2.2 0060 0060 0378 0534 1410 1410 1577 Batch 1 is valid until 30 September 2006 1053 1159,1197 2102 2102 1308 1798 hydroxydiphenylacetic acid (benzilic acid) 1798 (1R,3r,5S)-8-azabicyclo[3.2.1]oct-3-yl hydroxydiphenylacetate 1798 (1R,3r,5S)-3-hydroxyspiro[8-azoniabicyclo[3.2.1]octane-8,1'-pyr 1798 rolidinium] (2,4-diaminopyrimidin-5-yl)(3,4,5-trimethoxyphenyl)methanone 4-amino-5-(3,4,5-trimethoxybenzyl)pyrimidin-2-ol Batch 1 is valid until 30 April 2007 100% CÿH„NO– 1-phenyl-3-(piperidin-1-yl)propan-1-one Information Unit Sale Quantity Unit 300 μl 1 150 mg 1 40 mg 1 225 mg 1 n/a 1 2.5 ml 2 n/a 1 100 mg 1 50 mg 1 25 mg 1 2-hydroxy-4-(trifluoromethyl)benzoic acid; (4-(trifluoromethyl)salicylic acid) 6 December 2006 Valproic acid Vancomycin hydrochloride Vanillin Vecuronium bromide Vecuronium for peak identification Venlafaxine hydrochloride Venlafaxine for system suitability Verapamil hydrochloride Verapamil impurity I V0033000 V0045000 V0050000 Y0000561 Y0000625 Y0000587 Y0000588 V0100000 V0100018 © Council of Europe, all rights reserved 2006 V0100026 Verapamil impurity M Uracil arabinoside Urea Ursodeoxycholic acid Valerian standardised dry extract Valine Valnemulin hydrochloride Valnemulin hydrogen tartrate Valnemulin for peak identification Valnemulin impurity E Tyrothricin Ubidecarenone Ubidecarenone for system suitability Ubidecarenone impurity D T3000000 U0020000 U0020001 U0020008 U0100000 U0600000 U0800000 New Y0000583 V0030000 Y0000584 Y0000533 Y0000585 Y0000586 2 1 n/a 1 Tylosin D Tylosin phosphate for peak identification Tylosin tartrate - reference spectrum Tyrosine T2880100 Y0000498 T2880200 T2900000 2 2 2 1 1 1 1 1 1 2 1 2 1 1 1 1 1 1 1 1 1 1 1 1 1 1 T2610000 Tryptophan T2800000 Tubocurarine chloride T2880000 Tylosin Batch 2 Reference Standard Order Code T2600000 Trypsin BRP Catalogue No. 48-2006/4 20 mg 100 mg 100 mg 100 mg 10 mg 10 mg 50 mg 1 mg 100 mg 5 mg 30 mg 100 mg 60 mg 400 mg 50 mg 10 mg 120 mg 10.25 mg 10 mg 10 mg 50 mg 10 mg 5 mg 5 mg 10 mg n/a 50 mg 100 mg 100 mg 150 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 1 0760 0743 1189,1275 0453,1898,1899 0770,0771,0796 2137 2137 2137 2137 0476,0579,0580, 0694 1272 0305 1273,1274,1661, 20702 1273,1274,1661 1273,1274,1661 1274 0782,0895,1161, 1272,1384 0907,1662 1578 1578 1578 Monograph 58 Yes Yes Yes Yes Yes Yes +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C Leaflet Storage a a a a g g a a a a a a a c a a a a a a a a a a a l a a a a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a For extra charges please see 2.2 1378 102500 IU per vial 1058,20702 0747 1769 1769 2119 2119 0573 (2¢£)-2-(3,4-dimethoxyphenyl)-2-[2-[[2-(3,4)dimethoxyphenyl)- 0573 ethyl](methyl)amino]ethyl]-3-methylbutanenitrile 5,5'-[[2-(3,4)dimethoxyphenyl)ethyl]imino]bis[2-(3,4-dimethoxy 0573 -phenyl)-2-(1-methylethyl)pentanenitrile (3aS,4R,5S,6S,8R,9R,9aR,10R)-6-ethenyl-5-hydroxy-4,6,9,10-te tramethyl-1-oxodecahydro-3a,9-propano-3aH-cyclopenta[8]ann ulen-8-yl 2-hydroxyacetate (pleuromulin) 98.7% C–—H—‡NœOŒŒS 5,6-dimethoxy-3-methyl-2-[(all-E)-3,7,11,15,19,23,27,31,35nonamethylhexatriaconta-2,6,10,14,18,22,26,30,34-nonaenyl] benzene-1,4-dione (ubiquinone-9) 87.75% C–ŸH÷œClœNœOÿ 1035 IU per mg Information Unit Sale Quantity Unit 100 mg 1 0.707 microkatal per mg 6 December 2006 4 n/a 4 n/a 2 n/a 1 1 1 1 1 1 1 1 1 1 1 2 3 Zinc acexamate Zinc acexamate impurity A Zolpidem tartrate - * psy Zolpidem impurity A Zopiclone -* psy Zopiclone oxide Zuclopenthixol decanoate - reference spectrum Zuclopenthixol for system suitability Zuclopenthixol impurity B Z2000000 Z2000010 Z2500000 Z2500010 Z3000000 Z3001000 Y0000062 Y0000534 Y0000083 © Council of Europe, all rights reserved 2006 1 Z1904000 Zidovudine impurity B 1 2 n/a 1 1 1 1 2 X0200000 Xylose Z1900000 Zidovudine Z1902000 Zidovudine impurity A Vinblastine sulphate Vinblastine sulphate - reference spectrum Vincristine sulphate Vincristine sulphate - reference spectrum Vindesine sulphate Vindesine sulphate - reference spectrum Vinorelbine tartrate Vinorelbine impurity B Warfarin sodium Xylazine hydrochloride Xylazine impurity C Xylazine impurity E Xylitol Xylometazoline hydrochloride Xylometazoline impurity A V0300000 V0305000 V0400000 V0405000 V0500000 V0500010 Y0000463 Y0000464 W0100000 X0075000 Y0000158 Y0000159 X0080000 X0100000 X0101000 Batch 1 1 Reference Standard Order Code Y0000661 Verbenalin V0180000 VERO cells Catalogue No. 48-2006/4 60 mg 20 mg n/a 0.1 mg 10 mg 50 mg 50 mg 150 mg 10 mg 10 mg 100 mg 60 mg 10 mg 1 1 1 1 1 1 1 1 1 1 1 1 1 59 2-chloro-9H-thioxanthen-9-one N,N'-dimethyl-2-[7-methyl-2-(4-methylphenyl)imidazol[1,2-a] pyridin-3-yl]acetamide ; Batch 2 is valid until 31 January 2007 6-[[6-(acetylamino)hexanoyl]amino]hexanoic acid 1060 1060 1707 1707 1707 1279 1279 1280 1280 1278 99.7% CŒÕHŒ–N—O÷ 1059 1-[(2¢,5£)-5-hydroxymethyl-2,5-dihydro-2-furyl]-5-methyl 1059 pyrimidine-2,4(1§,3§)-dione 1-(3-chloro-2,3-dideoxy-ß-D-ribofuranosyl)-5-methylpyrimidine- 1059 2,4(1§,3§)-dione Yes Yes -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C +5°C +5°C +5°C +5°C +5°C +5°C +5°C -20°C -20°C -20°C +5°C -180°C Leaflet Storage j a l c a a a j a a a a a c l c l c l c c g a a a a g a 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 79 Extra Price charges 79 a 100 d For extra charges please see 2.2 Information Unit Sale Monograph Quantity Unit 11 mg 1 0.97 mg CŒŸHœ÷OŒÕ 1854 1 ml 2 Cell lines (kidney, african green monkey, Cercopithecus aethiops) 0213,0538,1057 titration of live measles, mumps and rubella vaccines 5 mg 1 5.01 mg per vial of C÷ÿHÿÕN÷OŒ–S 0748,0749 n/a 1 0748 4.98 mg 1 4.98 mg per vial of C÷ÿH—‡N÷OŒ÷S 0748,0749 n/a 1 0749 5 mg 1 5.11 mg of C÷–H—ŸN—OŒŒS 1276 n/a 1 1276 40 mg 1 2107 4-O-deacetylvinorelbine 7 mg 1 2107 100 mg 1 0698,0699 125 mg 1 1481 50 mg 1 2,6-dimethylphenyl isothiocyanate 1481 87.5% CŒÕHŒ–NSœ; N-(2,6-dimethylphenyl)-S-methyldithiourea 50 mg 1 1481 500 mg 1 99.2% C—HŒœO— 1381 100 mg 1 0972,1162 10 mg 1 N-(2-aminoethyl)-2-(4-1,1-dimethylethyl-2,6-dimethylphenyl) 1162 acetamide 6 December 2006
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