01 1ALEMBIC PHARMACEUTICALS LIMITED Vadodara IN
02 1CIPLA LIMITED Mumbai IN
03 1EMCURE PHARMACEUTICALS LIMITED Pune IN
04 1FORMOSA LABORATORIES, INC. Taoyuan TW
05 1MAPRIMED S.A. Buenos Aires AR
01 5Leflunomide
01 1Argentina
02 3India
03 1Taiwan
01 5Valid
Certificate Number : R1-CEP 2007-172 - Rev 02
Status : Valid
Issue Date : 2018-09-04
Type : Chemical
Substance Number : 2330
Certificate Number : R1-CEP 2007-050 - Rev 01
Status : Valid
Issue Date : 2014-07-28
Type : Chemical
Substance Number : 2330
Certificate Number : CEP 2018-269 - Rev 02
Status : Valid
Issue Date : 2024-09-11
Type : Chemical
Substance Number : 2330
Certificate Number : R1-CEP 2009-035 - Rev 01
Status : Valid
Issue Date : 2018-02-09
Type : Chemical
Substance Number : 2330
Certificate Number : R0-CEP 2018-252 - Rev 01
Status : Valid
Issue Date : 2022-10-27
Type : Chemical
Substance Number : 2330
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PharmaCompass offers a list of Leflunomide 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 Leflunomide manufacturer or Leflunomide supplier for your needs.
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A CAS-75706-12-6 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of CAS-75706-12-6, including repackagers and relabelers. The FDA regulates CAS-75706-12-6 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. CAS-75706-12-6 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 CAS-75706-12-6 supplier is an individual or a company that provides CAS-75706-12-6 active pharmaceutical ingredient (API) or CAS-75706-12-6 finished formulations upon request. The CAS-75706-12-6 suppliers may include CAS-75706-12-6 API manufacturers, exporters, distributors and traders.
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A CAS-75706-12-6 CEP of the European Pharmacopoeia monograph is often referred to as a CAS-75706-12-6 Certificate of Suitability (COS). The purpose of a CAS-75706-12-6 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of CAS-75706-12-6 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of CAS-75706-12-6 to their clients by showing that a CAS-75706-12-6 CEP has been issued for it. The manufacturer submits a CAS-75706-12-6 CEP (COS) as part of the market authorization procedure, and it takes on the role of a CAS-75706-12-6 CEP holder for the record. Additionally, the data presented in the CAS-75706-12-6 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the CAS-75706-12-6 DMF.
A CAS-75706-12-6 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. CAS-75706-12-6 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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