01 1M/s Mangalam Drugs and Organics Ltd
02 1M/s S Kant Healthcare ltd
01 1Dihydroartemisinin Ph. Int.
02 1Dihydroartemisinin Ph. Int.
01 1WC-0167
02 1WC-0319
01 2India
Date of Issue : 2022-10-27
Valid Till : 2025-07-22
Written Confirmation Number : WC-0167
Address of the Firm : Unit No.1, Plot No.187, IInd Phase, GIDC Vapi-396195, Dist-Valsad, India
Date of Issue : 2022-05-20
Valid Till : 2025-01-13
Written Confirmation Number : WC-0319
Address of the Firm : Plot no.1802-1805GIDC Phase III, Vapi 396195 Dist Valsad, Gujarat
A Dihydroartemisinin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dihydroartemisinin, including repackagers and relabelers. The FDA regulates Dihydroartemisinin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dihydroartemisinin API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Dihydroartemisinin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dihydroartemisinin supplier is an individual or a company that provides Dihydroartemisinin active pharmaceutical ingredient (API) or Dihydroartemisinin finished formulations upon request. The Dihydroartemisinin suppliers may include Dihydroartemisinin API manufacturers, exporters, distributors and traders.
click here to find a list of Dihydroartemisinin suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Dihydroartemisinin written confirmation (Dihydroartemisinin WC) is an official document issued by a regulatory agency to a Dihydroartemisinin manufacturer, verifying that the manufacturing facility of a Dihydroartemisinin active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Dihydroartemisinin APIs or Dihydroartemisinin finished pharmaceutical products to another nation, regulatory agencies frequently require a Dihydroartemisinin WC (written confirmation) as part of the regulatory process.
click here to find a list of Dihydroartemisinin suppliers with Written Confirmation (WC) on PharmaCompass.
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