01 1M/s Syngene International Limited
01 1Odevixibat Sesquihydrate IH
01 1WC-0502
01 1India
Date of Issue : 2021-07-14
Valid Till : 2024-07-13
Written Confirmation Number : WC-0502
Address of the Firm : Biocon Park, Plot No 2,3,4, Unit S14, IV Phase Bommasandra industrial area, Jiga...
A Odevixibat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Odevixibat, including repackagers and relabelers. The FDA regulates Odevixibat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Odevixibat 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 Odevixibat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Odevixibat supplier is an individual or a company that provides Odevixibat active pharmaceutical ingredient (API) or Odevixibat finished formulations upon request. The Odevixibat suppliers may include Odevixibat API manufacturers, exporters, distributors and traders.
click here to find a list of Odevixibat suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Odevixibat written confirmation (Odevixibat WC) is an official document issued by a regulatory agency to a Odevixibat manufacturer, verifying that the manufacturing facility of a Odevixibat active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Odevixibat APIs or Odevixibat finished pharmaceutical products to another nation, regulatory agencies frequently require a Odevixibat WC (written confirmation) as part of the regulatory process.
click here to find a list of Odevixibat suppliers with Written Confirmation (WC) on PharmaCompass.
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