01 1YUIL PHARM TECH. C.O. , LTD.
01 1Aprindine Hydrochloride
01 1Japan
Registration Number : 231MF10039
Registrant's Address : 3, Mulmi-gil, Iwol-myeon, Jincheon-gun, Chungcheongbuk-do, Republic of Korea
Initial Date of Registration : 2019-02-12
Latest Date of Registration : 2019-02-12
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PharmaCompass offers a list of Aprindine 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 Aprindine Hydrochloride manufacturer or Aprindine Hydrochloride supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Aprindine Hydrochloride manufacturer or Aprindine Hydrochloride supplier.
PharmaCompass also assists you with knowing the Aprindine Hydrochloride API Price utilized in the formulation of products. Aprindine Hydrochloride API Price is not always fixed or binding as the Aprindine Hydrochloride Price is obtained through a variety of data sources. The Aprindine Hydrochloride Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Fiboran manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fiboran, including repackagers and relabelers. The FDA regulates Fiboran manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fiboran API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
A Fiboran supplier is an individual or a company that provides Fiboran active pharmaceutical ingredient (API) or Fiboran finished formulations upon request. The Fiboran suppliers may include Fiboran API manufacturers, exporters, distributors and traders.
click here to find a list of Fiboran 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 Fiboran Drug Master File in Japan (Fiboran JDMF) empowers Fiboran 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 Fiboran JDMF during the approval evaluation for pharmaceutical products. At the time of Fiboran 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 Fiboran suppliers with JDMF on PharmaCompass.
