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Status : Withdrawn by EDQM Failure to CEP pro...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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cimetidine manufacturer or Cimetidine supplier.
PharmaCompass also assists you with knowing the Cimetidine API Price utilized in the formulation of products. Cimetidine API Price is not always fixed or binding as the Cimetidine Price is obtained through a variety of data sources. The Cimetidine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A FPF 1002 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of FPF 1002, including repackagers and relabelers. The FDA regulates FPF 1002 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. FPF 1002 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 FPF 1002 supplier is an individual or a company that provides FPF 1002 active pharmaceutical ingredient (API) or FPF 1002 finished formulations upon request. The FPF 1002 suppliers may include FPF 1002 API manufacturers, exporters, distributors and traders.
click here to find a list of FPF 1002 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A FPF 1002 CEP of the European Pharmacopoeia monograph is often referred to as a FPF 1002 Certificate of Suitability (COS). The purpose of a FPF 1002 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of FPF 1002 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of FPF 1002 to their clients by showing that a FPF 1002 CEP has been issued for it. The manufacturer submits a FPF 1002 CEP (COS) as part of the market authorization procedure, and it takes on the role of a FPF 1002 CEP holder for the record. Additionally, the data presented in the FPF 1002 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the FPF 1002 DMF.
A FPF 1002 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. FPF 1002 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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