Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
01 1ZHEJIANG HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
02 1BAYER AG Leverkusen DE
03 1SIEGFRIED AG Zofingen CH
04 1SIEGFRIED LTD Zofingen CH
05 1SIEGFRIED LTD. Zofingen CH
01 1Acemetacin
02 1Acemetacin, Code 100033
03 1Acemetacin, Polymorphic form II
04 1Acemetacin, Pubagang site
05 1Acemetacin, Unmilled, milled
01 1China
02 1Germany
03 3Switzerland
01 1Expired
02 3Valid
03 1Withdrawn by Holder
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
Certificate Number : R0-CEP 2022-226 - Rev 00
Status : Valid
Issue Date : 2022-11-10
Type : Chemical
Substance Number : 1686
Certificate Number : R0-CEP 2010-323 - Rev 02
Status : Expired
Issue Date : 2017-03-06
Type : Chemical
Substance Number : 1686
Certificate Number : R1-CEP 2012-211 - Rev 02
Status : Valid
Issue Date : 2021-04-19
Type : Chemical
Substance Number : 1686
Acemetacin, Polymorphic Form II
Certificate Number : CEP 2018-306 - Rev 01
Status : Valid
Issue Date : 2024-06-25
Type : Chemical
Substance Number : 1686
Certificate Number : R0-CEP 2009-366 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2012-02-16
Type : Chemical
Substance Number : 1686
69
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A Acemetacin intermuti manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Acemetacin intermuti, including repackagers and relabelers. The FDA regulates Acemetacin intermuti manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Acemetacin intermuti 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 Acemetacin intermuti supplier is an individual or a company that provides Acemetacin intermuti active pharmaceutical ingredient (API) or Acemetacin intermuti finished formulations upon request. The Acemetacin intermuti suppliers may include Acemetacin intermuti API manufacturers, exporters, distributors and traders.
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A Acemetacin intermuti CEP of the European Pharmacopoeia monograph is often referred to as a Acemetacin intermuti Certificate of Suitability (COS). The purpose of a Acemetacin intermuti CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Acemetacin intermuti EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Acemetacin intermuti to their clients by showing that a Acemetacin intermuti CEP has been issued for it. The manufacturer submits a Acemetacin intermuti CEP (COS) as part of the market authorization procedure, and it takes on the role of a Acemetacin intermuti CEP holder for the record. Additionally, the data presented in the Acemetacin intermuti CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Acemetacin intermuti DMF.
A Acemetacin intermuti CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Acemetacin intermuti 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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