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Status : Withdrawn by Holder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 05
Status : Valid
Issue Date : 2024-05-27
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Status : Withdrawn by EDQM Failure to CEP pro...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
98
PharmaCompass offers a list of Rifampin 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 Rifampin manufacturer or Rifampin supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Rifampin manufacturer or Rifampin supplier.
PharmaCompass also assists you with knowing the Rifampin API Price utilized in the formulation of products. Rifampin API Price is not always fixed or binding as the Rifampin Price is obtained through a variety of data sources. The Rifampin Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A RMP manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of RMP, including repackagers and relabelers. The FDA regulates RMP manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. RMP 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 RMP manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A RMP supplier is an individual or a company that provides RMP active pharmaceutical ingredient (API) or RMP finished formulations upon request. The RMP suppliers may include RMP API manufacturers, exporters, distributors and traders.
click here to find a list of RMP suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A RMP CEP of the European Pharmacopoeia monograph is often referred to as a RMP Certificate of Suitability (COS). The purpose of a RMP CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of RMP EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of RMP to their clients by showing that a RMP CEP has been issued for it. The manufacturer submits a RMP CEP (COS) as part of the market authorization procedure, and it takes on the role of a RMP CEP holder for the record. Additionally, the data presented in the RMP CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the RMP DMF.
A RMP CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. RMP 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 RMP suppliers with CEP (COS) on PharmaCompass.
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