01 1Fuji Chemical Industry Co., Ltd.
02 1Johko Pharmaceutical Co., Ltd.
03 1Katsura Chemical Co., Ltd.
04 1Tokuyama Corporation
01 2Nipradilol
02 1Nipradilol (production only)
03 1Nipragilol
01 4Japan
Nipradilol (for manufacturing only)
Registration Number : 221MF10264
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2009-12-07
Latest Date of Registration : 2009-12-07
Registration Number : 218MF10460
Registrant's Address : 4-15-19 Hibarigaoka, Zama City, Kanagawa Prefecture
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2007-01-10
Registration Number : 301MF10010
Registrant's Address : 5 Kajigaishi Nishi 1-chome, Kitanagoya City, Aichi Prefecture
Initial Date of Registration : 2019-05-31
Latest Date of Registration : 2020-07-09
Registration Number : 218MF10267
Registrant's Address : 1-1 Mikage-cho, Shunan City, Yamaguchi Prefecture
Initial Date of Registration : 2006-02-17
Latest Date of Registration : 2007-01-18
A Nipradilol manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Nipradilol, including repackagers and relabelers. The FDA regulates Nipradilol manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Nipradilol 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 Nipradilol manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Nipradilol supplier is an individual or a company that provides Nipradilol active pharmaceutical ingredient (API) or Nipradilol finished formulations upon request. The Nipradilol suppliers may include Nipradilol API manufacturers, exporters, distributors and traders.
click here to find a list of Nipradilol 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 Nipradilol Drug Master File in Japan (Nipradilol JDMF) empowers Nipradilol 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 Nipradilol JDMF during the approval evaluation for pharmaceutical products. At the time of Nipradilol 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 Nipradilol suppliers with JDMF on PharmaCompass.
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