01 1M/s. Suven Life Sciences Limited
01 1Rifapentin IH
01 1WC-0042
01 1India
Date of Issue : 2019-07-15
Valid Till : 2022-07-14
Written Confirmation Number : WC-0042
Address of the Firm : Plot No.262, 263, IDA, Pashamylaram, Medak District, A.P
A Rifapentine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Rifapentine, including repackagers and relabelers. The FDA regulates Rifapentine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Rifapentine 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 Rifapentine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Rifapentine supplier is an individual or a company that provides Rifapentine active pharmaceutical ingredient (API) or Rifapentine finished formulations upon request. The Rifapentine suppliers may include Rifapentine API manufacturers, exporters, distributors and traders.
click here to find a list of Rifapentine suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Rifapentine written confirmation (Rifapentine WC) is an official document issued by a regulatory agency to a Rifapentine manufacturer, verifying that the manufacturing facility of a Rifapentine active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Rifapentine APIs or Rifapentine finished pharmaceutical products to another nation, regulatory agencies frequently require a Rifapentine WC (written confirmation) as part of the regulatory process.
click here to find a list of Rifapentine suppliers with Written Confirmation (WC) on PharmaCompass.
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