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 Kelfer manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Kelfer, including repackagers and relabelers. The FDA regulates Kelfer manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Kelfer 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 Kelfer supplier is an individual or a company that provides Kelfer active pharmaceutical ingredient (API) or Kelfer finished formulations upon request. The Kelfer suppliers may include Kelfer API manufacturers, exporters, distributors and traders.
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A Kelfer written confirmation (Kelfer WC) is an official document issued by a regulatory agency to a Kelfer manufacturer, verifying that the manufacturing facility of a Kelfer active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Kelfer APIs or Kelfer finished pharmaceutical products to another nation, regulatory agencies frequently require a Kelfer WC (written confirmation) as part of the regulatory process.
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