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Status : Withdrawn by Holder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 : R1-CEP 1998-057 - Rev 05
Status : Valid
Issue Date : 2022-01-04
Type : Chemical
Substance Number : 1156
A Tenoxicam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tenoxicam, including repackagers and relabelers. The FDA regulates Tenoxicam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tenoxicam API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Tenoxicam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tenoxicam supplier is an individual or a company that provides Tenoxicam active pharmaceutical ingredient (API) or Tenoxicam finished formulations upon request. The Tenoxicam suppliers may include Tenoxicam API manufacturers, exporters, distributors and traders.
click here to find a list of Tenoxicam suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Tenoxicam CEP of the European Pharmacopoeia monograph is often referred to as a Tenoxicam Certificate of Suitability (COS). The purpose of a Tenoxicam CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Tenoxicam EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Tenoxicam to their clients by showing that a Tenoxicam CEP has been issued for it. The manufacturer submits a Tenoxicam CEP (COS) as part of the market authorization procedure, and it takes on the role of a Tenoxicam CEP holder for the record. Additionally, the data presented in the Tenoxicam CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Tenoxicam DMF.
A Tenoxicam CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Tenoxicam 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 Tenoxicam suppliers with CEP (COS) on PharmaCompass.
We have 3 companies offering Tenoxicam
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
