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 Granules India Limited
03 1M/s RPG Life Sciences Ltd
01 1Azathioprine BP/EP/USP
02 1Azathioprine Ph. Eur/BP/USP
03 1Azathioprine USP/EP
01 1WC-0024n
02 1WC-0056n
03 1WC-0099
01 3India
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...
Date of Issue : 2022-06-03
Valid Till : 2025-07-28
Written Confirmation Number : WC-0056n
Address of the Firm : 25 MIDC Land, Thane Belapur Road, Navi Mumbai - 400703, Taluka: Pawvane, Distric...
Date of Issue : 2022-08-07
Valid Till : 2025-06-26
Written Confirmation Number : WC-0024n
Address of the Firm : Plot No.8, Jawaharlal Nehru Pharmacity, Tadi (V) Paravada, Visakhapatnam-531 019...
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PharmaCompass offers a list of Azathioprine 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 Azathioprine manufacturer or Azathioprine supplier for your needs.
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A Imurel manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Imurel, including repackagers and relabelers. The FDA regulates Imurel manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Imurel 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 Imurel supplier is an individual or a company that provides Imurel active pharmaceutical ingredient (API) or Imurel finished formulations upon request. The Imurel suppliers may include Imurel API manufacturers, exporters, distributors and traders.
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A Imurel written confirmation (Imurel WC) is an official document issued by a regulatory agency to a Imurel manufacturer, verifying that the manufacturing facility of a Imurel active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Imurel APIs or Imurel finished pharmaceutical products to another nation, regulatory agencies frequently require a Imurel WC (written confirmation) as part of the regulatory process.
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