01 2Daiwa Pharmaceutical Industries Co., Ltd.
02 1ERREGIERRE S. p. A.
03 1Fuji Chemical Industry Co., Ltd.
01 1Duck Stat mesylate
02 1Duck Stat mesylate (production only)
03 1Japanese Pharmacopoeia duck Stat mesylate (production only)
04 1Japanese Pharmacopoeia mesylate camostat (production only)
01 1Italy
02 3Japan
Registration Number : 229MF10164
Registrant's Address : VIA F. BARACCA 19-24060 SAN PAOLO D'ARGON (BERGAMO) ITALY
Initial Date of Registration : 2017-08-22
Latest Date of Registration : 2024-11-20
Camostat mesilate (for manufacturing only)
Registration Number : 221MF10058
Registrant's Address : 55 Yokohoonji, Kamiichi-cho, Nakaniikawa-gun, Toyama Prefecture
Initial Date of Registration : 2009-03-19
Latest Date of Registration : 2009-03-19
Japanese Pharmacopoeia Camostat Mesilate (for manufacturing only)
Registration Number : 219MF10222
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2007-07-06
Latest Date of Registration : 2007-07-06
Japanese Pharmacopoeia Camostat Mesilate (for manufacturing only)
Registration Number : 218MF10465
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-04-27
Latest Date of Registration : 2006-04-27
A Camostat manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Camostat, including repackagers and relabelers. The FDA regulates Camostat manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Camostat 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 Camostat manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Camostat supplier is an individual or a company that provides Camostat active pharmaceutical ingredient (API) or Camostat finished formulations upon request. The Camostat suppliers may include Camostat API manufacturers, exporters, distributors and traders.
click here to find a list of Camostat 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 Camostat Drug Master File in Japan (Camostat JDMF) empowers Camostat 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 Camostat JDMF during the approval evaluation for pharmaceutical products. At the time of Camostat 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 Camostat suppliers with JDMF on PharmaCompass.
We have 3 companies offering Camostat
Get in contact with the supplier of your choice:
LOOKING FOR A SUPPLIER?
