01 1AMSA S. p. A.
01 1Flecainide acetate
01 1Italy
Registration Number : 223MF10093
Registrant's Address : VIALE DEL GHISALLO, 20 20151 MILAN ITALY
Initial Date of Registration : 2011-06-29
Latest Date of Registration : 2025-01-28
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PharmaCompass offers a list of Flecainide 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 Flecainide manufacturer or Flecainide supplier for your needs.
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PharmaCompass also assists you with knowing the Flecainide API Price utilized in the formulation of products. Flecainide API Price is not always fixed or binding as the Flecainide Price is obtained through a variety of data sources. The Flecainide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A E-0735 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of E-0735, including repackagers and relabelers. The FDA regulates E-0735 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. E-0735 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 E-0735 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A E-0735 supplier is an individual or a company that provides E-0735 active pharmaceutical ingredient (API) or E-0735 finished formulations upon request. The E-0735 suppliers may include E-0735 API manufacturers, exporters, distributors and traders.
click here to find a list of E-0735 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 E-0735 Drug Master File in Japan (E-0735 JDMF) empowers E-0735 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 E-0735 JDMF during the approval evaluation for pharmaceutical products. At the time of E-0735 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 E-0735 suppliers with JDMF on PharmaCompass.
