01 1M/s. Aurobindo Pharma Ltd., (Unit-XI),
01 1Clindamycin Hydrochloride (Ph. Eur)
01 1WC-0023
01 1India
Clindamycin Hydrochloride (Ph. Eur)
Date of Issue : 2019-06-26
Valid Till : 2022-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Sy.No.1/22, 2/1 To 5, 6 to 18, 61 to 69, Pydibhimavaram Village, Ranasthalam, Sr...
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A DUAC manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DUAC, including repackagers and relabelers. The FDA regulates DUAC manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DUAC 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 DUAC supplier is an individual or a company that provides DUAC active pharmaceutical ingredient (API) or DUAC finished formulations upon request. The DUAC suppliers may include DUAC API manufacturers, exporters, distributors and traders.
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A DUAC written confirmation (DUAC WC) is an official document issued by a regulatory agency to a DUAC manufacturer, verifying that the manufacturing facility of a DUAC active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting DUAC APIs or DUAC finished pharmaceutical products to another nation, regulatory agencies frequently require a DUAC WC (written confirmation) as part of the regulatory process.
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