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, Crystallized From Isopropanol
Certificate Number : R0-CEP 2001-371 - Rev 01
Status : Expired
Issue Date : 2004-11-09
Type : Chemical
Substance Number : 756
Cimetidine, Crystallised From Ethanol
Certificate Number : R0-CEP 2000-153 - 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Status : Withdrawn by EDQM Failure to CEP pro...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 Magicul manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Magicul, including repackagers and relabelers. The FDA regulates Magicul manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Magicul API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Magicul manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Magicul supplier is an individual or a company that provides Magicul active pharmaceutical ingredient (API) or Magicul finished formulations upon request. The Magicul suppliers may include Magicul API manufacturers, exporters, distributors and traders.
click here to find a list of Magicul suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Magicul CEP of the European Pharmacopoeia monograph is often referred to as a Magicul Certificate of Suitability (COS). The purpose of a Magicul CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Magicul EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Magicul to their clients by showing that a Magicul CEP has been issued for it. The manufacturer submits a Magicul CEP (COS) as part of the market authorization procedure, and it takes on the role of a Magicul CEP holder for the record. Additionally, the data presented in the Magicul CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Magicul DMF.
A Magicul CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Magicul CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
click here to find a list of Magicul suppliers with CEP (COS) on PharmaCompass.
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