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 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
03 1ESTEVE QUIMICA S.A. Barcelona ES
01 3Tenoxicam
01 1China
02 1Spain
03 1Sweden
01 2Valid
02 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 : R1-CEP 2011-331 - Rev 02
Status : Valid
Issue Date : 2019-11-18
Type : Chemical
Substance Number : 1156
Certificate Number : R1-CEP 1999-114 - Rev 02
Status : Withdrawn by Holder
Issue Date : 2009-07-09
Type : Chemical
Substance Number : 1156
Certificate Number : CEP 1998-057 - Rev 06
Status : Valid
Issue Date : 2025-04-02
Type : Chemical
Substance Number : 1156
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A Reutenox manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Reutenox, including repackagers and relabelers. The FDA regulates Reutenox manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Reutenox 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 Reutenox supplier is an individual or a company that provides Reutenox active pharmaceutical ingredient (API) or Reutenox finished formulations upon request. The Reutenox suppliers may include Reutenox API manufacturers, exporters, distributors and traders.
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A Reutenox CEP of the European Pharmacopoeia monograph is often referred to as a Reutenox Certificate of Suitability (COS). The purpose of a Reutenox CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Reutenox EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Reutenox to their clients by showing that a Reutenox CEP has been issued for it. The manufacturer submits a Reutenox CEP (COS) as part of the market authorization procedure, and it takes on the role of a Reutenox CEP holder for the record. Additionally, the data presented in the Reutenox CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Reutenox DMF.
A Reutenox CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Reutenox 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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