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 Surajlok Chemcials Pvt ltd
01 1Mercaptopurine EP/USP/BP
02 1Mercaptopurine IP/BP
01 1WC-0099
02 1WC-0435a
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 : 2019-01-21
Valid Till : 2022-01-20
Written Confirmation Number : WC-0435a
Address of the Firm : Plot No. T-6, M.I.D.C, Tarapur Industrial Area,\\r\\nBoisar, Dist- Thane -401506...
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A PURIXAN manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of PURIXAN, including repackagers and relabelers. The FDA regulates PURIXAN manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. PURIXAN 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 PURIXAN supplier is an individual or a company that provides PURIXAN active pharmaceutical ingredient (API) or PURIXAN finished formulations upon request. The PURIXAN suppliers may include PURIXAN API manufacturers, exporters, distributors and traders.
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A PURIXAN written confirmation (PURIXAN WC) is an official document issued by a regulatory agency to a PURIXAN manufacturer, verifying that the manufacturing facility of a PURIXAN active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting PURIXAN APIs or PURIXAN finished pharmaceutical products to another nation, regulatory agencies frequently require a PURIXAN WC (written confirmation) as part of the regulatory process.
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