Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
01 1M/s Century Pharmaceuticals Limited
01 1Oxytetracycline Hydrochloride BP/EP/USP
01 1WC-0293
01 1India
Century has been an API manufacturer for over 40 years & is the partner of choice for multipurpose custom manufacturing projects.
Oxytetracycline Hydrochloride BP/EP/USP
Date of Issue : 2025-10-07
Valid Till : 2028-10-06
Written Confirmation Number : WC-0293
Address of the Firm : 103-106, GIDC Halol, Dist.-Panchmahal, Pin-389350, Gujarat, India
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A Oxy-Rivo manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxy-Rivo, including repackagers and relabelers. The FDA regulates Oxy-Rivo manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxy-Rivo 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 Oxy-Rivo supplier is an individual or a company that provides Oxy-Rivo active pharmaceutical ingredient (API) or Oxy-Rivo finished formulations upon request. The Oxy-Rivo suppliers may include Oxy-Rivo API manufacturers, exporters, distributors and traders.
click here to find a list of Oxy-Rivo suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
A Oxy-Rivo written confirmation (Oxy-Rivo WC) is an official document issued by a regulatory agency to a Oxy-Rivo manufacturer, verifying that the manufacturing facility of a Oxy-Rivo active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxy-Rivo APIs or Oxy-Rivo finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxy-Rivo WC (written confirmation) as part of the regulatory process.
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