01 1M/sMacleods pharmaceuticals Limited
01 1Ethionamide BP/Ph.Eur
01 1WC-0079
01 1India
Date of Issue : 2022-09-07
Valid Till : 2025-07-02
Written Confirmation Number : WC-0079
Address of the Firm : Plot No. - 2209, G.I.D.C., Sarigam - 396 155, Dist - Valsad, Gujarat, India
69
PharmaCompass offers a list of Ethionamide 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 Ethionamide manufacturer or Ethionamide supplier for your needs.
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PharmaCompass also assists you with knowing the Ethionamide API Price utilized in the formulation of products. Ethionamide API Price is not always fixed or binding as the Ethionamide Price is obtained through a variety of data sources. The Ethionamide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Ethionamid prothionamid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Ethionamid prothionamid, including repackagers and relabelers. The FDA regulates Ethionamid prothionamid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Ethionamid prothionamid 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 Ethionamid prothionamid supplier is an individual or a company that provides Ethionamid prothionamid active pharmaceutical ingredient (API) or Ethionamid prothionamid finished formulations upon request. The Ethionamid prothionamid suppliers may include Ethionamid prothionamid API manufacturers, exporters, distributors and traders.
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A Ethionamid prothionamid written confirmation (Ethionamid prothionamid WC) is an official document issued by a regulatory agency to a Ethionamid prothionamid manufacturer, verifying that the manufacturing facility of a Ethionamid prothionamid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Ethionamid prothionamid APIs or Ethionamid prothionamid finished pharmaceutical products to another nation, regulatory agencies frequently require a Ethionamid prothionamid WC (written confirmation) as part of the regulatory process.
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