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
79
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A BROMFED-DM manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BROMFED-DM, including repackagers and relabelers. The FDA regulates BROMFED-DM manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BROMFED-DM 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 BROMFED-DM supplier is an individual or a company that provides BROMFED-DM active pharmaceutical ingredient (API) or BROMFED-DM finished formulations upon request. The BROMFED-DM suppliers may include BROMFED-DM API manufacturers, exporters, distributors and traders.
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A BROMFED-DM written confirmation (BROMFED-DM WC) is an official document issued by a regulatory agency to a BROMFED-DM manufacturer, verifying that the manufacturing facility of a BROMFED-DM active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BROMFED-DM APIs or BROMFED-DM finished pharmaceutical products to another nation, regulatory agencies frequently require a BROMFED-DM WC (written confirmation) as part of the regulatory process.
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