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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PharmaCompass offers a list of Tetracycline Hydrochloride API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,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.
PharmaCompass also assists you with knowing the Tetracycline Hydrochloride API Price utilized in the formulation of products. Tetracycline Hydrochloride API Price is not always fixed or binding as the Tetracycline Hydrochloride Price is obtained through a variety of data sources. The Tetracycline Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tetramed manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tetramed, including repackagers and relabelers. The FDA regulates Tetramed manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tetramed 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 Tetramed manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tetramed supplier is an individual or a company that provides Tetramed active pharmaceutical ingredient (API) or Tetramed finished formulations upon request. The Tetramed suppliers may include Tetramed API manufacturers, exporters, distributors and traders.
click here to find a list of Tetramed 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 Tetramed Drug Master File in Japan (Tetramed JDMF) empowers Tetramed 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 Tetramed JDMF during the approval evaluation for pharmaceutical products. At the time of Tetramed 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 Tetramed suppliers with JDMF on PharmaCompass.
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