Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1Aventis Bulk SpA - Subsidiary of Aventis Pharma Brindisi IT
02 1OLON S.P.A. Rodano IT
03 1Zhengzhou Minzhong Pharmaceutical Co., Ltd. Zhengzhou City CN
01 3Rifampicin
01 1China
02 1France
03 1Italy
01 1Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
Certificate Number : R0-CEP 2000-337 - Rev 03
Status : Withdrawn by Holder
Issue Date : 2005-02-18
Type : TSE
Substance Number : 52
Certificate Number : CEP 2009-275 - Rev 06
Status : Valid
Issue Date : 2026-02-18
Type : Chemical
Substance Number : 52
Certificate Number : R0-CEP 2004-295 - Rev 00
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-12-16
Type : Chemical
Substance Number : 52
96
PharmaCompass offers a list of Rifampicin 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 Rifampicin manufacturer or Rifampicin supplier for your needs.
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PharmaCompass also assists you with knowing the Rifampicin API Price utilized in the formulation of products. Rifampicin API Price is not always fixed or binding as the Rifampicin Price is obtained through a variety of data sources. The Rifampicin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A 8CI) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 8CI), including repackagers and relabelers. The FDA regulates 8CI) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 8CI) 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 8CI) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 8CI) supplier is an individual or a company that provides 8CI) active pharmaceutical ingredient (API) or 8CI) finished formulations upon request. The 8CI) suppliers may include 8CI) API manufacturers, exporters, distributors and traders.
click here to find a list of 8CI) suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A 8CI) CEP of the European Pharmacopoeia monograph is often referred to as a 8CI) Certificate of Suitability (COS). The purpose of a 8CI) CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of 8CI) EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of 8CI) to their clients by showing that a 8CI) CEP has been issued for it. The manufacturer submits a 8CI) CEP (COS) as part of the market authorization procedure, and it takes on the role of a 8CI) CEP holder for the record. Additionally, the data presented in the 8CI) CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the 8CI) DMF.
A 8CI) CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. 8CI) 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 8CI) suppliers with CEP (COS) on PharmaCompass.
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