01 1M/s. Mylan Laboratories Ltd.,
01 1Clindamycin Palmitate Hydrochloride (USP)
01 1WC-0118
01 1India
Clindamycin Palmitate Hydrochloride (USP)
Date of Issue : 2019-08-05
Valid Till : 2022-08-04
Written Confirmation Number : WC-0118
Address of the Firm : Unit -1, Sy No.10, Gaddapotharam (V), Khazipally Industrial Area,Medak Dist.,A.P...
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A Clindamycin Palmitate Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clindamycin Palmitate Hydrochloride, including repackagers and relabelers. The FDA regulates Clindamycin Palmitate Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clindamycin Palmitate Hydrochloride 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 Clindamycin Palmitate Hydrochloride supplier is an individual or a company that provides Clindamycin Palmitate Hydrochloride active pharmaceutical ingredient (API) or Clindamycin Palmitate Hydrochloride finished formulations upon request. The Clindamycin Palmitate Hydrochloride suppliers may include Clindamycin Palmitate Hydrochloride API manufacturers, exporters, distributors and traders.
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A Clindamycin Palmitate Hydrochloride written confirmation (Clindamycin Palmitate Hydrochloride WC) is an official document issued by a regulatory agency to a Clindamycin Palmitate Hydrochloride manufacturer, verifying that the manufacturing facility of a Clindamycin Palmitate Hydrochloride active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clindamycin Palmitate Hydrochloride APIs or Clindamycin Palmitate Hydrochloride finished pharmaceutical products to another nation, regulatory agencies frequently require a Clindamycin Palmitate Hydrochloride WC (written confirmation) as part of the regulatory process.
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