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 1Brompheniramine Maieate (USP/BP/EP)
02 1Brompheniramine Maleate (BP/EP/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.
Brompheniramine Maleate (BP/EP/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, ...
Brompheniramine Maieate (USP/BP/EP)
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
79
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A DIMETANE-DX manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DIMETANE-DX, including repackagers and relabelers. The FDA regulates DIMETANE-DX manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DIMETANE-DX 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-DX supplier is an individual or a company that provides DIMETANE-DX active pharmaceutical ingredient (API) or DIMETANE-DX finished formulations upon request. The DIMETANE-DX suppliers may include DIMETANE-DX API manufacturers, exporters, distributors and traders.
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A DIMETANE-DX written confirmation (DIMETANE-DX WC) is an official document issued by a regulatory agency to a DIMETANE-DX manufacturer, verifying that the manufacturing facility of a DIMETANE-DX active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DIMETANE-DX APIs or DIMETANE-DX finished pharmaceutical products to another nation, regulatory agencies frequently require a DIMETANE-DX WC (written confirmation) as part of the regulatory process.
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