Aarti Pharmalabs is a partner of choice for APIs & Intermediates and the largest Indian manufacturer of Xanthine Derivatives.
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01 1M/s. Aarti Pharmalabs Limited
02 1M/s RPG Life Sciences Limited
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01 1Azathioprine BP/EP/USP
02 1Azathioprine EP/BP/USP
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01 1WC-0056
02 1WC-0099
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01 2India
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...
Date of Issue : 2022-06-03
Valid Till : 2025-07-28
Written Confirmation Number : WC-0056
Address of the Firm : Plot No.2702, A, GIDC, Estate Ankleshwar, Dist Bharuch, Gujarat
39
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 azatiopr in manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of azatiopr in, including repackagers and relabelers. The FDA regulates azatiopr in manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. azatiopr in 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 azatiopr in supplier is an individual or a company that provides azatiopr in active pharmaceutical ingredient (API) or azatiopr in finished formulations upon request. The azatiopr in suppliers may include azatiopr in API manufacturers, exporters, distributors and traders.
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A azatiopr in written confirmation (azatiopr in WC) is an official document issued by a regulatory agency to a azatiopr in manufacturer, verifying that the manufacturing facility of a azatiopr in active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting azatiopr in APIs or azatiopr in finished pharmaceutical products to another nation, regulatory agencies frequently require a azatiopr in WC (written confirmation) as part of the regulatory process.
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