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 Chlorhydrate de tetracycline manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Chlorhydrate de tetracycline, including repackagers and relabelers. The FDA regulates Chlorhydrate de tetracycline manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Chlorhydrate de tetracycline API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Chlorhydrate de tetracycline supplier is an individual or a company that provides Chlorhydrate de tetracycline active pharmaceutical ingredient (API) or Chlorhydrate de tetracycline finished formulations upon request. The Chlorhydrate de tetracycline suppliers may include Chlorhydrate de tetracycline API manufacturers, exporters, distributors and traders.
click here to find a list of Chlorhydrate de tetracycline 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 Chlorhydrate de tetracycline Drug Master File in Japan (Chlorhydrate de tetracycline JDMF) empowers Chlorhydrate de tetracycline 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 Chlorhydrate de tetracycline JDMF during the approval evaluation for pharmaceutical products. At the time of Chlorhydrate de tetracycline 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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