01 1M/s. Ind- Swift Laboratories Limited
01 1Clarithromycin Citrate (IH)
01 1WC-0003
01 1India
Date of Issue : 2022-06-03
Valid Till : 2025-05-27
Written Confirmation Number : WC-0003
Address of the Firm : Vill.- Bhagwanpur, Barwala Road, Near Dera Bassi, Distt.- SAS Nagar (Mohali), Pu...
A UNII-16K08R7NG0 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of UNII-16K08R7NG0, including repackagers and relabelers. The FDA regulates UNII-16K08R7NG0 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. UNII-16K08R7NG0 API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A UNII-16K08R7NG0 supplier is an individual or a company that provides UNII-16K08R7NG0 active pharmaceutical ingredient (API) or UNII-16K08R7NG0 finished formulations upon request. The UNII-16K08R7NG0 suppliers may include UNII-16K08R7NG0 API manufacturers, exporters, distributors and traders.
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A UNII-16K08R7NG0 written confirmation (UNII-16K08R7NG0 WC) is an official document issued by a regulatory agency to a UNII-16K08R7NG0 manufacturer, verifying that the manufacturing facility of a UNII-16K08R7NG0 active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting UNII-16K08R7NG0 APIs or UNII-16K08R7NG0 finished pharmaceutical products to another nation, regulatory agencies frequently require a UNII-16K08R7NG0 WC (written confirmation) as part of the regulatory process.
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