Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
01 1DUKE CHEM, S.A.U. Olérdola ES
02 1BAYER AG Leverkusen DE
03 1DISHMAN CARBOGEN AMCIS LIMITED Ahmedabad IN
04 1ESTEVE QUIMICA S.A. Barcelona ES
01 4Etofenamate
01 1Germany
02 1India
03 2Spain
01 3Valid
02 1Withdrawn by Holder
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
Gentec Pharmaceutical Group is focused on manufacturing & developing APIs/HPAPIs, Advanced Intermediates & Fine Chemicals.
Certificate Number : CEP 2014-154 - Rev 01
Status : Valid
Issue Date : 2024-02-27
Type : Chemical
Substance Number : 1513
Certificate Number : R1-CEP 2006-158 - Rev 01
Status : Valid
Issue Date : 2017-03-06
Type : Chemical
Substance Number : 1513
Certificate Number : R0-CEP 2011-350 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2017-07-04
Type : Chemical
Substance Number : 1513
Certificate Number : R1-CEP 2012-114 - Rev 02
Status : Valid
Issue Date : 2022-03-16
Type : Chemical
Substance Number : 1513
A Etofenamate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Etofenamate, including repackagers and relabelers. The FDA regulates Etofenamate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Etofenamate 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 Etofenamate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Etofenamate supplier is an individual or a company that provides Etofenamate active pharmaceutical ingredient (API) or Etofenamate finished formulations upon request. The Etofenamate suppliers may include Etofenamate API manufacturers, exporters, distributors and traders.
click here to find a list of Etofenamate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Etofenamate CEP of the European Pharmacopoeia monograph is often referred to as a Etofenamate Certificate of Suitability (COS). The purpose of a Etofenamate CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Etofenamate EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Etofenamate to their clients by showing that a Etofenamate CEP has been issued for it. The manufacturer submits a Etofenamate CEP (COS) as part of the market authorization procedure, and it takes on the role of a Etofenamate CEP holder for the record. Additionally, the data presented in the Etofenamate CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Etofenamate DMF.
A Etofenamate CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Etofenamate 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 Etofenamate suppliers with CEP (COS) on PharmaCompass.
We have 4 companies offering Etofenamate
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