Century has been an API manufacturer for over 30 years & is the partner of choice for multipurpose custom manufacturing projects.
01 1M/s. Century Pharmaceuticals Limited
01 1Oxytetracycline USP, Oxytetracycline Dihydrate BP/EP
01 1WC-0293
01 1India
Century has been an API manufacturer for over 30 years & is the partner of choice for multipurpose custom manufacturing projects.
Oxytetracycline USP, Oxytetracycline Dihydrate BP/EP
Date of Issue : 2022-11-02
Valid Till : 2024-12-16
Written Confirmation Number : WC-0293
Address of the Firm : 103-106, GIDC Halol, Dist.-Panchmahal, Pin-389350, Gujarat
A Oxytetracycline Dihydrate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Oxytetracycline Dihydrate, including repackagers and relabelers. The FDA regulates Oxytetracycline Dihydrate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Oxytetracycline Dihydrate API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
click here to find a list of Oxytetracycline Dihydrate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Oxytetracycline Dihydrate supplier is an individual or a company that provides Oxytetracycline Dihydrate active pharmaceutical ingredient (API) or Oxytetracycline Dihydrate finished formulations upon request. The Oxytetracycline Dihydrate suppliers may include Oxytetracycline Dihydrate API manufacturers, exporters, distributors and traders.
click here to find a list of Oxytetracycline Dihydrate suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PharmaCompass.
A Oxytetracycline Dihydrate written confirmation (Oxytetracycline Dihydrate WC) is an official document issued by a regulatory agency to a Oxytetracycline Dihydrate manufacturer, verifying that the manufacturing facility of a Oxytetracycline Dihydrate active pharmaceutical ingredient (API) adheres to the Good Manufacturing Practices (GMP) regulations of the importing country. When exporting Oxytetracycline Dihydrate APIs or Oxytetracycline Dihydrate finished pharmaceutical products to another nation, regulatory agencies frequently require a Oxytetracycline Dihydrate WC (written confirmation) as part of the regulatory process.
click here to find a list of Oxytetracycline Dihydrate suppliers with Written Confirmation (WC) on PharmaCompass.
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