01 2Gedeon Richter Ltd Budapest HU
02 1JIANGSU ZENJI PHARMACEUTICALS LTD. Huai'an City CN
03 1Union Quimico Farmaceutica, S.A. (Uquifa S.A.) Barcelona ES
04 1Wuxi Kaili Pharmaceutical Co., Ltd. Yixing CN
01 3Cimetidine
02 1Cimetidine, Crystallised from ethanol
03 1Cimetidine, Crystallized from isopropanol
01 2China
02 2Hungary
03 1Spain
01 2Expired
02 2Valid
03 1Withdrawn by EDQM Failure to CEP procedure
Cimetidine, Crystallised From Ethanol
Certificate Number : R0-CEP 2000-153 - Rev 01
Status : Expired
Issue Date : 2004-11-09
Type : Chemical
Substance Number : 756
Cimetidine, Crystallized From Isopropanol
Certificate Number : R0-CEP 2001-371 - Rev 01
Status : Expired
Issue Date : 2004-11-09
Type : Chemical
Substance Number : 756
Certificate Number : R0-CEP 2020-301 - Rev 00
Status : Valid
Issue Date : 2023-06-27
Type : Chemical
Substance Number : 756
Certificate Number : R1-CEP 1998-023 - Rev 06
Status : Valid
Issue Date : 2019-09-03
Type : Chemical
Substance Number : 756
Certificate Number : R1-CEP 2002-008 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2010-04-27
Type : Chemical
Substance Number : 756
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PharmaCompass offers a list of Cimetidine API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Cimetidine manufacturer or Cimetidine supplier for your needs.
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A Tagamet Hb manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tagamet Hb, including repackagers and relabelers. The FDA regulates Tagamet Hb manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tagamet Hb API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Tagamet Hb supplier is an individual or a company that provides Tagamet Hb active pharmaceutical ingredient (API) or Tagamet Hb finished formulations upon request. The Tagamet Hb suppliers may include Tagamet Hb API manufacturers, exporters, distributors and traders.
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A Tagamet Hb CEP of the European Pharmacopoeia monograph is often referred to as a Tagamet Hb Certificate of Suitability (COS). The purpose of a Tagamet Hb CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tagamet Hb EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tagamet Hb to their clients by showing that a Tagamet Hb CEP has been issued for it. The manufacturer submits a Tagamet Hb CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tagamet Hb CEP holder for the record. Additionally, the data presented in the Tagamet Hb CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tagamet Hb DMF.
A Tagamet Hb CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tagamet Hb CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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