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
A Tetracycline Hydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetracycline Hydrochloride, including repackagers and relabelers. The FDA regulates Tetracycline Hydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetracycline Hydrochloride 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 Tetracycline Hydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetracycline Hydrochloride supplier is an individual or a company that provides Tetracycline Hydrochloride active pharmaceutical ingredient (API) or Tetracycline Hydrochloride finished formulations upon request. The Tetracycline Hydrochloride suppliers may include Tetracycline Hydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Tetracycline Hydrochloride suppliers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price 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 Tetracycline Hydrochloride Drug Master File in Japan (Tetracycline Hydrochloride JDMF) empowers Tetracycline Hydrochloride 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 Tetracycline Hydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Tetracycline Hydrochloride JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
click here to find a list of Tetracycline Hydrochloride suppliers with JDMF on PharmaCompass.
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