Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 1M/s Aarti Pharmalabs ltd
02 1M/s Alembic Pharmaceuticals Limited
03 1M/s Chemeca Drugs Private Limited
04 1M/s Chemino Pharma limited
05 1M/s Divi's Laboratories Limited
06 1M/s Hetero Drugs Limited
07 1M/s Hikal Limited
08 1M/s Hikal limited
09 1M/s Sun Pharmaceutical Industries Ltd
10 1M/s. Glenmark Life Sciences Limited
11 1M/sCadila Pharmaceuticals Ltd
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2022-08-24
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: Palghar, Di...
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PharmaCompass offers a list of Bupropion Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Bupropion Hydrochloride manufacturer or Bupropion Hydrochloride supplier for your needs.
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A Voxra manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Voxra, including repackagers and relabelers. The FDA regulates Voxra manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Voxra 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 Voxra supplier is an individual or a company that provides Voxra active pharmaceutical ingredient (API) or Voxra finished formulations upon request. The Voxra suppliers may include Voxra API manufacturers, exporters, distributors and traders.
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A Voxra written confirmation (Voxra WC) is an official document issued by a regulatory agency to a Voxra manufacturer, verifying that the manufacturing facility of a Voxra active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Voxra APIs or Voxra finished pharmaceutical products to another nation, regulatory agencies frequently require a Voxra WC (written confirmation) as part of the regulatory process.
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