01 1M/s. Amsal Chem Pvt., Ltd.,
02 1M/s. Calyx Chemicals and Pharmaceuticals Ltd.,
01 1Isoniazid (BP/ EP/USP)
02 1Isoniazid BP/EP/USP
01 1WC-0088
02 1WC-0172
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.
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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 Isotamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Isotamine, including repackagers and relabelers. The FDA regulates Isotamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Isotamine 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 Isotamine supplier is an individual or a company that provides Isotamine active pharmaceutical ingredient (API) or Isotamine finished formulations upon request. The Isotamine suppliers may include Isotamine API manufacturers, exporters, distributors and traders.
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A Isotamine written confirmation (Isotamine WC) is an official document issued by a regulatory agency to a Isotamine manufacturer, verifying that the manufacturing facility of a Isotamine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Isotamine APIs or Isotamine finished pharmaceutical products to another nation, regulatory agencies frequently require a Isotamine WC (written confirmation) as part of the regulatory process.
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