01 1M/s Lupin Limited
01 1Cephalexin USP
01 1WC-0202
01 1India
Date of Issue : 2025-10-08
Valid Till : 2028-07-04
Written Confirmation Number : WC-0202
Address of the Firm : 198-202, New Industrial Area No.2, Mandideep-462046 Goharganj, Raisen-462046, Di...
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A Keflet manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Keflet, including repackagers and relabelers. The FDA regulates Keflet manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Keflet 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 Keflet manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Keflet supplier is an individual or a company that provides Keflet active pharmaceutical ingredient (API) or Keflet finished formulations upon request. The Keflet suppliers may include Keflet API manufacturers, exporters, distributors and traders.
click here to find a list of Keflet suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Keflet written confirmation (Keflet WC) is an official document issued by a regulatory agency to a Keflet manufacturer, verifying that the manufacturing facility of a Keflet active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Keflet APIs or Keflet finished pharmaceutical products to another nation, regulatory agencies frequently require a Keflet WC (written confirmation) as part of the regulatory process.
click here to find a list of Keflet suppliers with Written Confirmation (WC) on PharmaCompass.
