01 1M/s IPCA Laboratories Ltd
02 1M/s Megafine Pharma P Limited
01 1Pyrantel Embonate BP/Ph. Eur
02 1Pyrantel Pamoate IP/USP
01 1WC-0087
02 1WC-0091
01 2India
Date of Issue : 2025-06-19
Valid Till : 2028-07-02
Written Confirmation Number : WC-0091
Address of the Firm : P.O. Sejavta, District -Ratlam, (M.P.)-457001, India
Date of Issue : 2025-10-01
Valid Till : 2028-07-02
Written Confirmation Number : WC-0087
Address of the Firm : Plot No.1 to 5, 31 to 35 & 48 to 51, 26 & Kl201, Village Lakhmapur, Taluka Dindo...
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A Nemocid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nemocid, including repackagers and relabelers. The FDA regulates Nemocid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nemocid 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 Nemocid supplier is an individual or a company that provides Nemocid active pharmaceutical ingredient (API) or Nemocid finished formulations upon request. The Nemocid suppliers may include Nemocid API manufacturers, exporters, distributors and traders.
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A Nemocid written confirmation (Nemocid WC) is an official document issued by a regulatory agency to a Nemocid manufacturer, verifying that the manufacturing facility of a Nemocid active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Nemocid APIs or Nemocid finished pharmaceutical products to another nation, regulatory agencies frequently require a Nemocid WC (written confirmation) as part of the regulatory process.
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