Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 2M/s Supriya Lifescience Ltd
02 1Keshava Organics
01 3Brompheniramine Maleate BP/EP/USP
01 2WC-0218n
02 1WC-0244
01 3India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Brompheniramine Maleate BP/EP/USP
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218n
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Brompheniramine Maleate BP/EP/USP
Date of Issue : 2022-06-29
Valid Till : 2025-07-02
Written Confirmation Number : WC-0218n
Address of the Firm : A-5/2, Late Parshuram Industrial Area, MIDC, Tal-Khed, Dist. Ratnagiri-415 722, ...
Brompheniramine Maleate BP/EP/USP
Date of Issue : 2022-12-09
Valid Till : 2025-07-02
Written Confirmation Number : WC-0244
Address of the Firm : Plot No. T-97 & 100, MIDC, Tarapur, -401 506, Taluka: Palghar, Dist-Thane Zone-4
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A Dimetane Extentabs manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dimetane Extentabs, including repackagers and relabelers. The FDA regulates Dimetane Extentabs manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dimetane Extentabs 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 Dimetane Extentabs supplier is an individual or a company that provides Dimetane Extentabs active pharmaceutical ingredient (API) or Dimetane Extentabs finished formulations upon request. The Dimetane Extentabs suppliers may include Dimetane Extentabs API manufacturers, exporters, distributors and traders.
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A Dimetane Extentabs written confirmation (Dimetane Extentabs WC) is an official document issued by a regulatory agency to a Dimetane Extentabs manufacturer, verifying that the manufacturing facility of a Dimetane Extentabs active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dimetane Extentabs APIs or Dimetane Extentabs finished pharmaceutical products to another nation, regulatory agencies frequently require a Dimetane Extentabs WC (written confirmation) as part of the regulatory process.
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