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