01 1Oril Industry
01 1Trimetazidine hydrochloride
01 1France
Registration Number : 222MF10081
Registrant's Address : 13, rue Auguste Desgene(') tais, 76210 Bolbec, FRANCE
Initial Date of Registration : 2010-03-09
Latest Date of Registration : 2010-03-09
A Trimetazidine Dihydrochloride manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Trimetazidine Dihydrochloride, including repackagers and relabelers. The FDA regulates Trimetazidine Dihydrochloride manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Trimetazidine Dihydrochloride 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 Trimetazidine Dihydrochloride manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Trimetazidine Dihydrochloride supplier is an individual or a company that provides Trimetazidine Dihydrochloride active pharmaceutical ingredient (API) or Trimetazidine Dihydrochloride finished formulations upon request. The Trimetazidine Dihydrochloride suppliers may include Trimetazidine Dihydrochloride API manufacturers, exporters, distributors and traders.
click here to find a list of Trimetazidine Dihydrochloride 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 Trimetazidine Dihydrochloride Drug Master File in Japan (Trimetazidine Dihydrochloride JDMF) empowers Trimetazidine Dihydrochloride 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 Trimetazidine Dihydrochloride JDMF during the approval evaluation for pharmaceutical products. At the time of Trimetazidine Dihydrochloride 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 Trimetazidine Dihydrochloride suppliers with JDMF on PharmaCompass.
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