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Status : Withdrawn by Holder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Status : Withdrawn by EDQM Failure to CEP pro...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 Tubocin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tubocin, including repackagers and relabelers. The FDA regulates Tubocin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tubocin 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 Tubocin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tubocin supplier is an individual or a company that provides Tubocin active pharmaceutical ingredient (API) or Tubocin finished formulations upon request. The Tubocin suppliers may include Tubocin API manufacturers, exporters, distributors and traders.
click here to find a list of Tubocin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tubocin CEP of the European Pharmacopoeia monograph is often referred to as a Tubocin Certificate of Suitability (COS). The purpose of a Tubocin CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tubocin EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tubocin to their clients by showing that a Tubocin CEP has been issued for it. The manufacturer submits a Tubocin CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tubocin CEP holder for the record. Additionally, the data presented in the Tubocin CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tubocin DMF.
A Tubocin CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tubocin 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 Tubocin suppliers with CEP (COS) on PharmaCompass.
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