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01 1M/s Emcure Pharmaceuticals Ltd
02 1M/s. Alembic Pharmaceuticals Limited,
03 1M/s. Cipla Limited
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01 1Leflunomide (EP)
02 1Leflunomide (USP/BP/Ph.Eur)
03 1Leflunomide USP, Ph.Eur
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01 1WC-0081
02 1WC-0113
03 1WC-0226
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01 3India
Date of Issue : 2019-07-05
Valid Till : 2022-07-02
Written Confirmation Number : WC-0081
Address of the Firm : (API Division Panelav), Panelav, Tal-Halol, Dist-Panchmahal, Gujarat, India
Date of Issue : 2022-06-20
Valid Till : 2025-08-08
Written Confirmation Number : WC-0113
Address of the Firm : Old Madras Road, Virgo Nagar Post, Bengaluru - 560049
Date of Issue : 2019-10-07
Valid Till : 2022-07-02
Written Confirmation Number : WC-0226
Address of the Firm : D-24 and D24/1 MIDC Kurkumbh Tal. Daund, Dist Pune 413 802, Maharashtra State
45
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 written confirmation (EU-0100649 WC) is an official document issued by a regulatory agency to a EU-0100649 manufacturer, verifying that the manufacturing facility of a EU-0100649 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting EU-0100649 APIs or EU-0100649 finished pharmaceutical products to another nation, regulatory agencies frequently require a EU-0100649 WC (written confirmation) as part of the regulatory process.
click here to find a list of EU-0100649 suppliers with Written Confirmation (WC) on PharmaCompass.
We have 3 companies offering EU-0100649
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