01 1M/s Mehta API Pvt Ltd
01 1Prochlorperazine Mesylate BP
01 1WC-0214
01 1India
Date of Issue : 2022-10-14
Valid Till : 2025-07-02
Written Confirmation Number : WC-0214
Address of the Firm : Gut No. 546,571,519 and 520, Village Kumbhavali, Boisar, Tal & Dist- Palghar, Pi...
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PharmaCompass offers a list of Prochlorperazine 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 Prochlorperazine manufacturer or Prochlorperazine supplier for your needs.
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A Stemetil manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Stemetil, including repackagers and relabelers. The FDA regulates Stemetil manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Stemetil 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 Stemetil supplier is an individual or a company that provides Stemetil active pharmaceutical ingredient (API) or Stemetil finished formulations upon request. The Stemetil suppliers may include Stemetil API manufacturers, exporters, distributors and traders.
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A Stemetil written confirmation (Stemetil WC) is an official document issued by a regulatory agency to a Stemetil manufacturer, verifying that the manufacturing facility of a Stemetil active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Stemetil APIs or Stemetil finished pharmaceutical products to another nation, regulatory agencies frequently require a Stemetil WC (written confirmation) as part of the regulatory process.
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