01 1M/s. Orchid Pharma Limited
01 1Cefoxitin Sodium (Sterile) Ph. Eur
01 1WC-0131
01 1India
Cefoxitin Sodium (Sterile) Ph. Eur
Date of Issue : 2025-08-01
Valid Till : 2028-07-21
Written Confirmation Number : WC-0131
Address of the Firm : Plot No.121-128, 128A-133,138-151 & 159-164,\\nSIDCO Industrial Estate Alathur,\...
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A DSSTox_CID_28921 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DSSTox_CID_28921, including repackagers and relabelers. The FDA regulates DSSTox_CID_28921 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DSSTox_CID_28921 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 DSSTox_CID_28921 supplier is an individual or a company that provides DSSTox_CID_28921 active pharmaceutical ingredient (API) or DSSTox_CID_28921 finished formulations upon request. The DSSTox_CID_28921 suppliers may include DSSTox_CID_28921 API manufacturers, exporters, distributors and traders.
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A DSSTox_CID_28921 written confirmation (DSSTox_CID_28921 WC) is an official document issued by a regulatory agency to a DSSTox_CID_28921 manufacturer, verifying that the manufacturing facility of a DSSTox_CID_28921 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DSSTox_CID_28921 APIs or DSSTox_CID_28921 finished pharmaceutical products to another nation, regulatory agencies frequently require a DSSTox_CID_28921 WC (written confirmation) as part of the regulatory process.
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