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Status : Withdrawn by EDQM Failure to CEP pro...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Status : Withdrawn by Holder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
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PharmaCompass offers a list of Triflusal 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 Triflusal manufacturer or Triflusal supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Triflusal manufacturer or Triflusal supplier.
PharmaCompass also assists you with knowing the Triflusal API Price utilized in the formulation of products. Triflusal API Price is not always fixed or binding as the Triflusal Price is obtained through a variety of data sources. The Triflusal Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Disgren manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Disgren, including repackagers and relabelers. The FDA regulates Disgren manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Disgren 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 Disgren manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Disgren supplier is an individual or a company that provides Disgren active pharmaceutical ingredient (API) or Disgren finished formulations upon request. The Disgren suppliers may include Disgren API manufacturers, exporters, distributors and traders.
click here to find a list of Disgren suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Disgren CEP of the European Pharmacopoeia monograph is often referred to as a Disgren Certificate of Suitability (COS). The purpose of a Disgren CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of Disgren EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of Disgren to their clients by showing that a Disgren CEP has been issued for it. The manufacturer submits a Disgren CEP (COS) as part of the market authorization procedure, and it takes on the role of a Disgren CEP holder for the record. Additionally, the data presented in the Disgren CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the Disgren DMF.
A Disgren CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. Disgren 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 Disgren suppliers with CEP (COS) on PharmaCompass.
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