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, ...
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PharmaCompass also assists you with knowing the Dexbrompheniramine Maleate API Price utilized in the formulation of products. Dexbrompheniramine Maleate API Price is not always fixed or binding as the Dexbrompheniramine Maleate Price is obtained through a variety of data sources. The Dexbrompheniramine Maleate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dexbrompheniramine Maleate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dexbrompheniramine Maleate, including repackagers and relabelers. The FDA regulates Dexbrompheniramine Maleate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dexbrompheniramine 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.
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A Dexbrompheniramine Maleate supplier is an individual or a company that provides Dexbrompheniramine Maleate active pharmaceutical ingredient (API) or Dexbrompheniramine Maleate finished formulations upon request. The Dexbrompheniramine Maleate suppliers may include Dexbrompheniramine Maleate API manufacturers, exporters, distributors and traders.
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A Dexbrompheniramine Maleate written confirmation (Dexbrompheniramine Maleate WC) is an official document issued by a regulatory agency to a Dexbrompheniramine Maleate manufacturer, verifying that the manufacturing facility of a Dexbrompheniramine Maleate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dexbrompheniramine Maleate APIs or Dexbrompheniramine Maleate finished pharmaceutical products to another nation, regulatory agencies frequently require a Dexbrompheniramine Maleate WC (written confirmation) as part of the regulatory process.
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