01 1M/s Apothecon Pharmaceuticals Pvt. Ltd
01 1Salcaprozate Sodium IH
01 1WC-0369
01 1India
Date of Issue : 2026-03-16
Valid Till : 2029-03-16
Written Confirmation Number : WC-0369
Address of the Firm : Plot No. 1134, 1135, 1136, 1137,1143B, 1144 A&B, 1138 A&B, Padra -Jambusar Highw...
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A Salcaprozate Sodium manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Salcaprozate Sodium, including repackagers and relabelers. The FDA regulates Salcaprozate Sodium manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Salcaprozate Sodium 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 Salcaprozate Sodium supplier is an individual or a company that provides Salcaprozate Sodium active pharmaceutical ingredient (API) or Salcaprozate Sodium finished formulations upon request. The Salcaprozate Sodium suppliers may include Salcaprozate Sodium API manufacturers, exporters, distributors and traders.
click here to find a list of Salcaprozate Sodium suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Salcaprozate Sodium written confirmation (Salcaprozate Sodium WC) is an official document issued by a regulatory agency to a Salcaprozate Sodium manufacturer, verifying that the manufacturing facility of a Salcaprozate Sodium active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Salcaprozate Sodium APIs or Salcaprozate Sodium finished pharmaceutical products to another nation, regulatory agencies frequently require a Salcaprozate Sodium WC (written confirmation) as part of the regulatory process.
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