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