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 Cipla Limited
03 1M/s.Srini Pharmaceuticals Private Limited
01 1Deferiprone IH
02 1Deferiprone IH/Ph. Eur
03 1Deferiprone Ph. Eur
01 1WC-0140
02 1WC-0295
03 1WC-0313
01 3India
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 : 2027-05-19
Written Confirmation Number : WC-0295
Address of the Firm : D-53, PHASE II, KALYAN SHILL ROAD, DOMBIVLI (E.), DOMBIVLI - 421204, Taluka: Dom...
Date of Issue : 2022-06-03
Valid Till : 2025-07-02
Written Confirmation Number : WC-0140
Address of the Firm : D-22, MIDC, Industrial Area, Kurkumbh, Tal-Daund, Dist- Pune- 413 802, Maharasht...
Date of Issue : 2023-07-10
Valid Till : 2025-05-21
Written Confirmation Number : WC-0313
Address of the Firm : SurveyNo.247,Choutuppal, Choutuppal (V),Choutuppal (M),YadadriBhuvanagiri Distri...
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A BP-12415 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of BP-12415, including repackagers and relabelers. The FDA regulates BP-12415 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. BP-12415 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 BP-12415 supplier is an individual or a company that provides BP-12415 active pharmaceutical ingredient (API) or BP-12415 finished formulations upon request. The BP-12415 suppliers may include BP-12415 API manufacturers, exporters, distributors and traders.
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A BP-12415 written confirmation (BP-12415 WC) is an official document issued by a regulatory agency to a BP-12415 manufacturer, verifying that the manufacturing facility of a BP-12415 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting BP-12415 APIs or BP-12415 finished pharmaceutical products to another nation, regulatory agencies frequently require a BP-12415 WC (written confirmation) as part of the regulatory process.
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