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
56
PharmaCompass offers a list of Tetracycline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, and more, enabling you to easily find the right Tetracycline Hydrochloride manufacturer or Tetracycline Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tetracycline Hydrochloride manufacturer or Tetracycline Hydrochloride supplier.
A Unicin manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Unicin, including repackagers and relabelers. The FDA regulates Unicin manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Unicin 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 Unicin manufacturers with USDMF, JDMF, KDMF, CEP, GMP, and COA related information on PhamaCompass.
A Unicin supplier is an individual or a company that provides Unicin active pharmaceutical ingredient (API) or Unicin finished formulations upon request. The Unicin suppliers may include Unicin API manufacturers, exporters, distributors and traders.
click here to find a list of Unicin 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 Unicin Drug Master File in Japan (Unicin JDMF) empowers Unicin 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 Unicin JDMF during the approval evaluation for pharmaceutical products. At the time of Unicin 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 Unicin suppliers with JDMF on PharmaCompass.
We have 1 companies offering Unicin
Get in contact with the supplier of your choice:
