01 1Cambrex Profarmaco Milano S. r. l.
02 1DNP Fine Chemicals Utsunomiya Co., Ltd.
01 2Flunitrazepam
01 1Japan
02 1U.S.A
Registration Number : 217MF11256
Registrant's Address : Via Curiel 34, 20067 Paulo, Milano, ITALY
Initial Date of Registration : 2005-12-20
Latest Date of Registration : 2020-09-17
Registration Number : 231MF10063
Registrant's Address : 1062-8 Honjo, Nishikata-cho, Tochigi City, Tochigi Prefecture
Initial Date of Registration : 2019-03-04
Latest Date of Registration : 2019-03-04
A Flunitrazepam manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flunitrazepam, including repackagers and relabelers. The FDA regulates Flunitrazepam manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flunitrazepam 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 Flunitrazepam manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flunitrazepam supplier is an individual or a company that provides Flunitrazepam active pharmaceutical ingredient (API) or Flunitrazepam finished formulations upon request. The Flunitrazepam suppliers may include Flunitrazepam API manufacturers, exporters, distributors and traders.
click here to find a list of Flunitrazepam 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 Flunitrazepam Drug Master File in Japan (Flunitrazepam JDMF) empowers Flunitrazepam 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 Flunitrazepam JDMF during the approval evaluation for pharmaceutical products. At the time of Flunitrazepam 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 Flunitrazepam suppliers with JDMF on PharmaCompass.
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