01 1ESTEVE QUIMICA S.A. Barcelona ES
02 1Estechpharma Co., Ltd. Kyonggi-do KR
03 1INFAR, S.A. Palafolls ES
04 1URQUIMA S.A. Palau-solità i Plegamans ES
01 4Triflusal
01 1South Korea
02 3Spain
01 2Valid
02 1Withdrawn by EDQM Failure to CEP procedure
03 1Withdrawn by Holder
Certificate Number : R1-CEP 2004-195 - Rev 01
Status : Withdrawn by EDQM Failure to CEP pro...
Issue Date : 2012-01-13
Type : Chemical
Substance Number : 1377
Certificate Number : R0-CEP 2002-135 - Rev 01
Status : Withdrawn by Holder
Issue Date : 2004-10-18
Type : Chemical
Substance Number : 1377
Certificate Number : R1-CEP 2015-326 - Rev 00
Status : Valid
Issue Date : 2021-12-10
Type : Chemical
Substance Number : 1377
Certificate Number : R1-CEP 2000-032 - Rev 04
Status : Valid
Issue Date : 2019-08-14
Type : Chemical
Substance Number : 1377
A Triflusal manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Triflusal, including repackagers and relabelers. The FDA regulates Triflusal manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Triflusal 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 Triflusal manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Triflusal supplier is an individual or a company that provides Triflusal active pharmaceutical ingredient (API) or Triflusal finished formulations upon request. The Triflusal suppliers may include Triflusal API manufacturers, exporters, distributors and traders.
click here to find a list of Triflusal suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Triflusal CEP of the European Pharmacopoeia monograph is often referred to as a Triflusal Certificate of Suitability (COS). The purpose of a Triflusal CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Triflusal EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Triflusal to their clients by showing that a Triflusal CEP has been issued for it. The manufacturer submits a Triflusal CEP (COS) as part of the market authorization procedure, and it takes on the role of a Triflusal CEP holder for the record. Additionally, the data presented in the Triflusal CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Triflusal DMF.
A Triflusal CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Triflusal 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 Triflusal suppliers with CEP (COS) on PharmaCompass.
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