01 1M/s. Apitoria Pharma Private Limited
01 1Clindamycin Palmitate Hydrochloride IH
01 1WC-0023
01 1India
Clindamycin Palmitate Hydrochloride IH
Date of Issue : 2022-06-07
Valid Till : 2025-06-25
Written Confirmation Number : WC-0023
Address of the Firm : Survey no. 52,53,58,59,61 to 78,127&128, Pydibhimanvaram Village &Sy.No. 1,2,4t0...
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PharmaCompass offers a list of Clindamycin Palmitate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Clindamycin Palmitate manufacturer or Clindamycin Palmitate supplier for your needs.
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A Cleocin palmitate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cleocin palmitate, including repackagers and relabelers. The FDA regulates Cleocin palmitate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cleocin palmitate 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 Cleocin palmitate supplier is an individual or a company that provides Cleocin palmitate active pharmaceutical ingredient (API) or Cleocin palmitate finished formulations upon request. The Cleocin palmitate suppliers may include Cleocin palmitate API manufacturers, exporters, distributors and traders.
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A Cleocin palmitate written confirmation (Cleocin palmitate WC) is an official document issued by a regulatory agency to a Cleocin palmitate manufacturer, verifying that the manufacturing facility of a Cleocin palmitate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Cleocin palmitate APIs or Cleocin palmitate finished pharmaceutical products to another nation, regulatory agencies frequently require a Cleocin palmitate WC (written confirmation) as part of the regulatory process.
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