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. Cadila Healthcare Limited,
03 1M/s. Cipla Ltd.
01 1Deferiprone EP
02 2Deferiprone IH
01 1WC-0084
02 1WC-0140
03 1WC-295
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 : 2027-05-20
Written Confirmation Number : WC-295
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, Kurkumbh, Dist. Pune-413 802
Date of Issue : 2019-07-15
Valid Till : 2022-07-14
Written Confirmation Number : WC-0084
Address of the Firm : Plot No 26, 29 & 31, Umraya Road, Village Dabhasa, Tal -Padra- 381 440, Vadodara...
A Deferiprone manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Deferiprone, including repackagers and relabelers. The FDA regulates Deferiprone manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Deferiprone 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 Deferiprone supplier is an individual or a company that provides Deferiprone active pharmaceutical ingredient (API) or Deferiprone finished formulations upon request. The Deferiprone suppliers may include Deferiprone API manufacturers, exporters, distributors and traders.
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A Deferiprone written confirmation (Deferiprone WC) is an official document issued by a regulatory agency to a Deferiprone manufacturer, verifying that the manufacturing facility of a Deferiprone active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Deferiprone APIs or Deferiprone finished pharmaceutical products to another nation, regulatory agencies frequently require a Deferiprone WC (written confirmation) as part of the regulatory process.
click here to find a list of Deferiprone suppliers with Written Confirmation (WC) on PharmaCompass.
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