Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.
01 1SANOFI CHIMIE Gentilly FR
02 1CENTAUR PHARMACEUTICALS PRIVATE LIMITED Mumbai IN
03 1CENTIPHARM Grasse FR
04 2F.I.S. - FABBRICA ITALIANA SINTETICI S.P.A. Montecchio Maggiore IT
01 4Tetrazepam
02 1Tetrazepam, Process 2
01 2France
02 1India
03 2Italy
01 1Valid
02 4Withdrawn 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 2008-288 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2010-07-27
Type : Chemical
Substance Number : 1738
Certificate Number : R0-CEP 2011-186 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-06-08
Type : Chemical
Substance Number : 1738
Certificate Number : R1-CEP 2007-003 - Rev 00
Status : Valid
Issue Date : 2013-01-29
Type : Chemical
Substance Number : 1738
Certificate Number : R1-CEP 2012-097 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2017-10-05
Type : Chemical
Substance Number : 1738
Certificate Number : R1-CEP 2008-152 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2015-02-13
Type : Chemical
Substance Number : 1738
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PharmaCompass offers a list of Tetrazepam 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 Tetrazepam manufacturer or Tetrazepam supplier for your needs.
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PharmaCompass also assists you with knowing the Tetrazepam API Price utilized in the formulation of products. Tetrazepam API Price is not always fixed or binding as the Tetrazepam Price is obtained through a variety of data sources. The Tetrazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Musaril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Musaril, including repackagers and relabelers. The FDA regulates Musaril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Musaril API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Musaril supplier is an individual or a company that provides Musaril active pharmaceutical ingredient (API) or Musaril finished formulations upon request. The Musaril suppliers may include Musaril API manufacturers, exporters, distributors and traders.
click here to find a list of Musaril suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Musaril CEP of the European Pharmacopoeia monograph is often referred to as a Musaril Certificate of Suitability (COS). The purpose of a Musaril CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Musaril EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Musaril to their clients by showing that a Musaril CEP has been issued for it. The manufacturer submits a Musaril CEP (COS) as part of the market authorization procedure, and it takes on the role of a Musaril CEP holder for the record. Additionally, the data presented in the Musaril CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Musaril DMF.
A Musaril CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Musaril 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 Musaril suppliers with CEP (COS) on PharmaCompass.
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