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.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Leflunomide manufacturer or Leflunomide supplier.
PharmaCompass also assists you with knowing the Leflunomide API Price utilized in the formulation of products. Leflunomide API Price is not always fixed or binding as the Leflunomide Price is obtained through a variety of data sources. The Leflunomide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A EU-0100649 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of EU-0100649, including repackagers and relabelers. The FDA regulates EU-0100649 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. EU-0100649 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 EU-0100649 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A EU-0100649 supplier is an individual or a company that provides EU-0100649 active pharmaceutical ingredient (API) or EU-0100649 finished formulations upon request. The EU-0100649 suppliers may include EU-0100649 API manufacturers, exporters, distributors and traders.
click here to find a list of EU-0100649 suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A EU-0100649 CEP of the European Pharmacopoeia monograph is often referred to as a EU-0100649 Certificate of Suitability (COS). The purpose of a EU-0100649 CEP is to show that the European Pharmacopoeia monograph adequately controls the purity of EU-0100649 EP produced by a given manufacturer. Suppliers of raw materials can prove the suitability of EU-0100649 to their clients by showing that a EU-0100649 CEP has been issued for it. The manufacturer submits a EU-0100649 CEP (COS) as part of the market authorization procedure, and it takes on the role of a EU-0100649 CEP holder for the record. Additionally, the data presented in the EU-0100649 CEP (COS) is managed confidentially and offers a centralized system acknowledged by numerous nations, exactly like the EU-0100649 DMF.
A EU-0100649 CEP (COS) is recognised by all 36 nations that make up the European Pharmacopoeia Convention. EU-0100649 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 EU-0100649 suppliers with CEP (COS) on PharmaCompass.
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