01 1M/s. Apicore Pharmaceuticals Pvt. Ltd.,
01 1Phentolamine Mesylate USP
01 1WC-0110n
01 1India
Date of Issue : 2022-07-15
Valid Till : 2025-07-02
Written Confirmation Number : WC-0110n
Address of the Firm : 252-253, Dhobikuva-391 440, Opp.Jain Irrigation, Padra Jambusar Highway, Tal.Pad...
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PharmaCompass offers a list of Phentolamine Mesylate 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 Phentolamine Mesylate manufacturer or Phentolamine Mesylate supplier for your needs.
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A Fentolamin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fentolamin, including repackagers and relabelers. The FDA regulates Fentolamin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fentolamin 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 Fentolamin supplier is an individual or a company that provides Fentolamin active pharmaceutical ingredient (API) or Fentolamin finished formulations upon request. The Fentolamin suppliers may include Fentolamin API manufacturers, exporters, distributors and traders.
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A Fentolamin written confirmation (Fentolamin WC) is an official document issued by a regulatory agency to a Fentolamin manufacturer, verifying that the manufacturing facility of a Fentolamin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Fentolamin APIs or Fentolamin finished pharmaceutical products to another nation, regulatory agencies frequently require a Fentolamin WC (written confirmation) as part of the regulatory process.
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