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01 1M/s. Amsal Chem Pvt., Ltd.,
02 1M/s. Calyx Chemicals and Pharmaceuticals Ltd.,
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01 1Isoniazid (BP/ EP/USP)
02 1Isoniazid BP/EP/USP
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01 1WC-0088
02 1WC-0172
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01 2India
Date of Issue : 2022-12-02
Valid Till : 2025-07-02
Written Confirmation Number : WC-0172
Address of the Firm : A-1, 401, 402 & 403 GIDC Ankleshwar, Bharuch India
Date of Issue : 2023-03-24
Valid Till : 2025-09-08
Written Confirmation Number : WC-0088
Address of the Firm : Plot No.N-102/91, 90 MIDC, Tarapur, Boisar, Palghar-401 506, Maharashtra, India
72
PharmaCompass offers a list of Isoniazid 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 Isoniazid manufacturer or Isoniazid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Isoniazid manufacturer or Isoniazid supplier.
PharmaCompass also assists you with knowing the Isoniazid API Price utilized in the formulation of products. Isoniazid API Price is not always fixed or binding as the Isoniazid Price is obtained through a variety of data sources. The Isoniazid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A rimif on manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of rimif on, including repackagers and relabelers. The FDA regulates rimif on manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. rimif on 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 rimif on supplier is an individual or a company that provides rimif on active pharmaceutical ingredient (API) or rimif on finished formulations upon request. The rimif on suppliers may include rimif on API manufacturers, exporters, distributors and traders.
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A rimif on written confirmation (rimif on WC) is an official document issued by a regulatory agency to a rimif on manufacturer, verifying that the manufacturing facility of a rimif on active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting rimif on APIs or rimif on finished pharmaceutical products to another nation, regulatory agencies frequently require a rimif on WC (written confirmation) as part of the regulatory process.
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