Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifesience Ltd
02 1M/s. Keshav Organics Pvt.Ltd
01 1Mepyramine Maieate (BP/EP)/Pyrilamine Maleate USP
02 1Mepyramine Maleate (BP/EP)/Pyrilamine Maleate USP
01 1WC-0218
02 1WC-244
01 2India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Mepyramine Maleate (BP/EP)/Pyrilamine Maleate USP
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Mepyramine Maieate (BP/EP)/Pyrilamine Maleate USP
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-244
Address of the Firm : Plot No. T-97 &T-100, MIDC Tarapur, Dist Thane-401506, Maharshtra
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A Prefrin A manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Prefrin A, including repackagers and relabelers. The FDA regulates Prefrin A manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Prefrin A 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 Prefrin A supplier is an individual or a company that provides Prefrin A active pharmaceutical ingredient (API) or Prefrin A finished formulations upon request. The Prefrin A suppliers may include Prefrin A API manufacturers, exporters, distributors and traders.
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A Prefrin A written confirmation (Prefrin A WC) is an official document issued by a regulatory agency to a Prefrin A manufacturer, verifying that the manufacturing facility of a Prefrin A active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Prefrin A APIs or Prefrin A finished pharmaceutical products to another nation, regulatory agencies frequently require a Prefrin A WC (written confirmation) as part of the regulatory process.
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