01 1Ace Japan Co., Ltd.
02 1JW Pharmaceutical Corporation
03 1Katsura Chemical Co., Ltd.
01 1AZOSEMIDE
02 2Azosemide
01 2Japan
02 1South Korea
Registration Number : 217MF10134
Registrant's Address : Yamagata Prefecture Higashine City Higashine City 5850-1
Initial Date of Registration : 2005-05-24
Latest Date of Registration : 2006-06-09
Registration Number : 228MF10203
Registrant's Address : 2477, Nambusunhwan-ro, Seocho-gu, Seoul Republic of Korea
Initial Date of Registration : 2016-10-31
Latest Date of Registration : 2016-10-31
Registration Number : 221MF10250
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2009-11-24
Latest Date of Registration : 2015-01-05
A Azosemide manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Azosemide, including repackagers and relabelers. The FDA regulates Azosemide manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Azosemide 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 Azosemide manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Azosemide supplier is an individual or a company that provides Azosemide active pharmaceutical ingredient (API) or Azosemide finished formulations upon request. The Azosemide suppliers may include Azosemide API manufacturers, exporters, distributors and traders.
click here to find a list of Azosemide 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 Azosemide Drug Master File in Japan (Azosemide JDMF) empowers Azosemide 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 Azosemide JDMF during the approval evaluation for pharmaceutical products. At the time of Azosemide 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 Azosemide suppliers with JDMF on PharmaCompass.
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