Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
01 2M/s. Aarti Pharmalabs Limited
02 2M/s Glenmark Life Sciences Limited
03 1M/s Melody Healthcare Pvt Ltd
04 1M/s. Aurobindo Pharma Ltd.,
05 1M/s. Hetero Drugs Limited, Unit -I
06 1M/s. Mylan Laboratories Ltd.,
07 1M/s. Piramal Enterprises Limited
08 1M/s. Apotex Pharmachem India Pvt. Ltd.,
Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
Date of Issue : 2024-05-20
Valid Till : 2027-05-20
Written Confirmation Number : WC-295
Address of the Firm : D-53, Phase II, Kalyan Shill Road, Dombivli (E.), Dombivli - 421204, Taluka: Dom...
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...
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A Perindopril Erbumine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Perindopril Erbumine, including repackagers and relabelers. The FDA regulates Perindopril Erbumine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Perindopril Erbumine 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 Perindopril Erbumine supplier is an individual or a company that provides Perindopril Erbumine active pharmaceutical ingredient (API) or Perindopril Erbumine finished formulations upon request. The Perindopril Erbumine suppliers may include Perindopril Erbumine API manufacturers, exporters, distributors and traders.
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A Perindopril Erbumine written confirmation (Perindopril Erbumine WC) is an official document issued by a regulatory agency to a Perindopril Erbumine manufacturer, verifying that the manufacturing facility of a Perindopril Erbumine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Perindopril Erbumine APIs or Perindopril Erbumine finished pharmaceutical products to another nation, regulatory agencies frequently require a Perindopril Erbumine WC (written confirmation) as part of the regulatory process.
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