01 1Arevipharma GmbH
01 1Torasemide
01 1Germany
Registration Number : 223MF10112
Registrant's Address : Meissner Strasse 35 D-01445 Radebeul, Germany
Initial Date of Registration : 2011-07-19
Latest Date of Registration : 2025-01-09
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PharmaCompass offers a list of Torsemide 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 Torsemide manufacturer or Torsemide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Torsemide manufacturer or Torsemide supplier.
PharmaCompass also assists you with knowing the Torsemide API Price utilized in the formulation of products. Torsemide API Price is not always fixed or binding as the Torsemide Price is obtained through a variety of data sources. The Torsemide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Sutril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sutril, including repackagers and relabelers. The FDA regulates Sutril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sutril 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 Sutril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Sutril supplier is an individual or a company that provides Sutril active pharmaceutical ingredient (API) or Sutril finished formulations upon request. The Sutril suppliers may include Sutril API manufacturers, exporters, distributors and traders.
click here to find a list of Sutril 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 Sutril Drug Master File in Japan (Sutril JDMF) empowers Sutril 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 Sutril JDMF during the approval evaluation for pharmaceutical products. At the time of Sutril 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 Sutril suppliers with JDMF on PharmaCompass.
