Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
01 1M/s Supriya Lifesience Ltd
01 1Dexbrompheniramine Maleate USP
01 1WC-0218
01 1India
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
Dexbrompheniramine 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, ...
A (+)-Brompheniramine maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of (+)-Brompheniramine maleate, including repackagers and relabelers. The FDA regulates (+)-Brompheniramine maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. (+)-Brompheniramine maleate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of (+)-Brompheniramine maleate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A (+)-Brompheniramine maleate supplier is an individual or a company that provides (+)-Brompheniramine maleate active pharmaceutical ingredient (API) or (+)-Brompheniramine maleate finished formulations upon request. The (+)-Brompheniramine maleate suppliers may include (+)-Brompheniramine maleate API manufacturers, exporters, distributors and traders.
click here to find a list of (+)-Brompheniramine maleate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A (+)-Brompheniramine maleate written confirmation ((+)-Brompheniramine maleate WC) is an official document issued by a regulatory agency to a (+)-Brompheniramine maleate manufacturer, verifying that the manufacturing facility of a (+)-Brompheniramine maleate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting (+)-Brompheniramine maleate APIs or (+)-Brompheniramine maleate finished pharmaceutical products to another nation, regulatory agencies frequently require a (+)-Brompheniramine maleate WC (written confirmation) as part of the regulatory process.
click here to find a list of (+)-Brompheniramine maleate suppliers with Written Confirmation (WC) on PharmaCompass.
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