01 1F. I. S. Fabrica Italiana Sintetici S. p. A.
01 1Flurazepam hydrochloride
01 1Italy
Registration Number : 218MF10792
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2006-10-06
Latest Date of Registration : 2006-10-06
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PharmaCompass offers a list of Flurazepam 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 Flurazepam manufacturer or Flurazepam supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flurazepam manufacturer or Flurazepam supplier.
PharmaCompass also assists you with knowing the Flurazepam API Price utilized in the formulation of products. Flurazepam API Price is not always fixed or binding as the Flurazepam Price is obtained through a variety of data sources. The Flurazepam Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Felison manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Felison, including repackagers and relabelers. The FDA regulates Felison manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Felison 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 Felison supplier is an individual or a company that provides Felison active pharmaceutical ingredient (API) or Felison finished formulations upon request. The Felison suppliers may include Felison API manufacturers, exporters, distributors and traders.
click here to find a list of Felison 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 Felison Drug Master File in Japan (Felison JDMF) empowers Felison 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 Felison JDMF during the approval evaluation for pharmaceutical products. At the time of Felison 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 Felison suppliers with JDMF on PharmaCompass.
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