Zhejiang Hengkang Pharm Group is a dynamic pharmaceutical entity, spanning drug research, large-scale production, and global marketing.
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01 1ZHEJIANG HENGKANG PHARMACEUTICAL CO., LTD. Sanmen CN
02 1EDMOND PHARMA S.R.L. Paderno Dugnano IT
03 1ESTEVE QUIMICA S.A. Barcelona ES
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01 3Tenoxicam
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01 1China
02 1Spain
03 1Sweden
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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Status : Withdrawn by Holder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 : R1-CEP 1998-057 - Rev 05
Status : Valid
Issue Date : 2022-01-04
Type : Chemical
Substance Number : 1156
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PharmaCompass offers a list of Tenoxicam 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 Tenoxicam manufacturer or Tenoxicam supplier for your needs.
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A Tilcotil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tilcotil, including repackagers and relabelers. The FDA regulates Tilcotil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tilcotil 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 Tilcotil supplier is an individual or a company that provides Tilcotil active pharmaceutical ingredient (API) or Tilcotil finished formulations upon request. The Tilcotil suppliers may include Tilcotil API manufacturers, exporters, distributors and traders.
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A Tilcotil CEP of the European Pharmacopoeia monograph is often referred to as a Tilcotil Certificate of Suitability (COS). The purpose of a Tilcotil CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tilcotil EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tilcotil to their clients by showing that a Tilcotil CEP has been issued for it. The manufacturer submits a Tilcotil CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tilcotil CEP holder for the record. Additionally, the data presented in the Tilcotil CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tilcotil DMF.
A Tilcotil CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tilcotil 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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