Sanofi is a pioneer in Diabetes Solutions, Human Vaccines, Innovative Drugs, Consumer Healthcare, and the new Genzyme.

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01 1Aventis Pharma Deutschland GmbH Frankfurt Am Main DE
02 1SHANDONG XINHUA PHARMACEUTICAL CO., LTD. Zibo CN
03 1VANI PHARMA LABS LIMITED Hyderabad IN
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01 3Propyphenazone
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01 1China
02 1France
03 1India
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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 : R1-CEP 1998-088 - Rev 00
Status : Withdrawn by Holder
Issue Date : 2004-12-07
Type : Chemical
Substance Number : 636
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Certificate Number : R1-CEP 2003-059 - Rev 05
Status : Valid
Issue Date : 2022-03-14
Type : Chemical
Substance Number : 636

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Certificate Number : R1-CEP 2001-041 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2008-01-23
Type : Chemical
Substance Number : 636

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PharmaCompass offers a list of Propyphenazone API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Propyphenazone manufacturer or Propyphenazone supplier for your needs.
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A Causyth manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Causyth, including repackagers and relabelers. The FDA regulates Causyth manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Causyth API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Causyth supplier is an individual or a company that provides Causyth active pharmaceutical ingredient (API) or Causyth finished formulations upon request. The Causyth suppliers may include Causyth API manufacturers, exporters, distributors and traders.
click here to find a list of Causyth suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Causyth CEP of the European Pharmacopoeia monograph is often referred to as a Causyth Certificate of Suitability (COS). The purpose of a Causyth CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Causyth EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Causyth to their clients by showing that a Causyth CEP has been issued for it. The manufacturer submits a Causyth CEP (COS) as part of the market authorization procedure, and it takes on the role of a Causyth CEP holder for the record. Additionally, the data presented in the Causyth CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Causyth DMF.
A Causyth CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Causyth CEPs may be accepted in nations that are not members of the Ph. Eur. at the discretion of the authorities there.
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