01 1Ningxia Qiyuan Pharmaceutical Co. , Ltd.
01 1Tetracycline hydrochloride
01 1China
Registration Number : 218MF11005
Registrant's Address : No. 1 Qiyuan Street, Wangyuan Industrial Area, Yinchuan City, Ningxia, 750101, P. R. ...
Initial Date of Registration : 2006-12-18
Latest Date of Registration : 2019-12-10
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A Supramycin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Supramycin, including repackagers and relabelers. The FDA regulates Supramycin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Supramycin 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 Supramycin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Supramycin supplier is an individual or a company that provides Supramycin active pharmaceutical ingredient (API) or Supramycin finished formulations upon request. The Supramycin suppliers may include Supramycin API manufacturers, exporters, distributors and traders.
click here to find a list of Supramycin suppliers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PharmaCompass.
The Pharmaceuticals and Medical Devices Agency (PMDA) established the Japan Drug Master File (JDMF), also known as the Master File (MF), to permit Japanese and foreign manufacturers of drug substances, intermediates, excipients, raw materials, and packaging materials (‘Products’) to voluntarily register confidential information about the production and management of their products in Japan.
The Supramycin Drug Master File in Japan (Supramycin JDMF) empowers Supramycin API manufacturers to present comprehensive information (e.g., production methods, data, etc.) to the review authority, i.e., PMDA (Pharmaceuticals & Medical Devices Agency).
PMDA reviews the Supramycin JDMF during the approval evaluation for pharmaceutical products. At the time of Supramycin JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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