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 HCl manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clindamycin Palmitate HCl, including repackagers and relabelers. The FDA regulates Clindamycin Palmitate HCl manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clindamycin Palmitate HCl 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 HCl supplier is an individual or a company that provides Clindamycin Palmitate HCl active pharmaceutical ingredient (API) or Clindamycin Palmitate HCl finished formulations upon request. The Clindamycin Palmitate HCl suppliers may include Clindamycin Palmitate HCl API manufacturers, exporters, distributors and traders.
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A Clindamycin Palmitate HCl written confirmation (Clindamycin Palmitate HCl WC) is an official document issued by a regulatory agency to a Clindamycin Palmitate HCl manufacturer, verifying that the manufacturing facility of a Clindamycin Palmitate HCl active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clindamycin Palmitate HCl APIs or Clindamycin Palmitate HCl finished pharmaceutical products to another nation, regulatory agencies frequently require a Clindamycin Palmitate HCl WC (written confirmation) as part of the regulatory process.
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