EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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 1France
02 2India
03 1Italy
EUROAPI, the leading small molecules API player, provides both API sales & CDMO services.
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
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
A Diumide-K manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Diumide-K, including repackagers and relabelers. The FDA regulates Diumide-K manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Diumide-K 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 Diumide-K manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Diumide-K supplier is an individual or a company that provides Diumide-K active pharmaceutical ingredient (API) or Diumide-K finished formulations upon request. The Diumide-K suppliers may include Diumide-K API manufacturers, exporters, distributors and traders.
click here to find a list of Diumide-K 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 Diumide-K Drug Master File in Japan (Diumide-K JDMF) empowers Diumide-K 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 Diumide-K JDMF during the approval evaluation for pharmaceutical products. At the time of Diumide-K 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 Diumide-K suppliers with JDMF on PharmaCompass.
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