Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s. Aarti Pharmalabs Limited
02 1M/s Supriya Lifesience Ltd
03 1M/s Chemeca Drugs
04 1M/s Chemino Pharma Limited
05 1M/s Glenmark Life Sciences Limited
06 1M/s Hikal Limited
07 1M/s Jubilant Pharmova Limited
08 1M/s. Alembic Pharmaceuticals Limited,
09 1M/s. Cadila Pharmaceuticals Ltd.,
10 1M/s. Hetero Drugs Limited
11 1M/s. Sun Pharmaceuticals Industries Ltd.
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2023-01-06
Valid Till : 2025-07-29
Written Confirmation Number : WC-0099
Address of the Firm : Plot No. E-50, 50/1 and 59/1, Unit — IV, MIDC, Tarapur — 401506, Taluka: Pal...
Supriya Lifesciences is a cGMP-compliant API manufacturing organization with a leadership position across key & niche products.
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 Bupropion Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Bupropion Hydrochloride, including repackagers and relabelers. The FDA regulates Bupropion Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Bupropion Hydrochloride 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 Bupropion Hydrochloride supplier is an individual or a company that provides Bupropion Hydrochloride active pharmaceutical ingredient (API) or Bupropion Hydrochloride finished formulations upon request. The Bupropion Hydrochloride suppliers may include Bupropion Hydrochloride API manufacturers, exporters, distributors and traders.
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A Bupropion Hydrochloride written confirmation (Bupropion Hydrochloride WC) is an official document issued by a regulatory agency to a Bupropion Hydrochloride manufacturer, verifying that the manufacturing facility of a Bupropion Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Bupropion Hydrochloride APIs or Bupropion Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Bupropion Hydrochloride WC (written confirmation) as part of the regulatory process.
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