01 1EUROAPI Germany GmbH
02 1F. I. S. Fabrica Italiana Sintetici S. p. A.
03 2Ipca Laboratories Limited
01 1"Japan-station" furosemide (production only)
02 3Furosemide
01 1Gabon
02 2India
03 1Italy
Registration Number : 217MF10541
Registrant's Address : Viale Milano 26 36075 Montecchio Maggiore Vicenza, Italy
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2023-11-08
Registration Number : 225MF10191
Registrant's Address : 48, Kandivli Industrial Estate, Kandivli (W), Mumbai 400 067, India
Initial Date of Registration : 2013-10-09
Latest Date of Registration : 2013-10-09
"JP" Furosemide (for manufacturing purposes only)
Registration Number : 218MF10276
Registrant's Address : 48, Kandivli Industrial Estate. Kandivli (W), Mumbai 400 067 India
Initial Date of Registration : 2006-02-23
Latest Date of Registration : 2007-01-22
Registration Number : 221MF10215
Registrant's Address : Brueningstrasse 50, 65926 Frankfurt am Main, Germany
Initial Date of Registration : 2009-09-28
Latest Date of Registration : 2017-03-07
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PharmaCompass offers a list of Furosemide 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 Furosemide manufacturer or Furosemide supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Furosemide manufacturer or Furosemide supplier.
PharmaCompass also assists you with knowing the Furosemide API Price utilized in the formulation of products. Furosemide API Price is not always fixed or binding as the Furosemide Price is obtained through a variety of data sources. The Furosemide Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Diusemide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diusemide, including repackagers and relabelers. The FDA regulates Diusemide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diusemide 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 Diusemide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diusemide supplier is an individual or a company that provides Diusemide active pharmaceutical ingredient (API) or Diusemide finished formulations upon request. The Diusemide suppliers may include Diusemide API manufacturers, exporters, distributors and traders.
click here to find a list of Diusemide 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 Diusemide Drug Master File in Japan (Diusemide JDMF) empowers Diusemide 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 Diusemide JDMF during the approval evaluation for pharmaceutical products. At the time of Diusemide 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 Diusemide suppliers with JDMF on PharmaCompass.
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