01 1M/s. Cadila Healthcare Limited,
01 1Clindamycin Phosphate USP/EP/BP
01 1WC-0084
01 1India
Clindamycin Phosphate USP/EP/BP
Date of Issue : 2019-07-15
Valid Till : 2022-07-14
Written Confirmation Number : WC-0084
Address of the Firm : Plot No 26, 29 & 31, Umraya Road, Village Dabhasa, Tal -Padra- 381 440, Vadodara...
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A Clindamax manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Clindamax, including repackagers and relabelers. The FDA regulates Clindamax manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Clindamax 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 Clindamax supplier is an individual or a company that provides Clindamax active pharmaceutical ingredient (API) or Clindamax finished formulations upon request. The Clindamax suppliers may include Clindamax API manufacturers, exporters, distributors and traders.
click here to find a list of Clindamax suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Clindamax written confirmation (Clindamax WC) is an official document issued by a regulatory agency to a Clindamax manufacturer, verifying that the manufacturing facility of a Clindamax active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Clindamax APIs or Clindamax finished pharmaceutical products to another nation, regulatory agencies frequently require a Clindamax WC (written confirmation) as part of the regulatory process.
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