01 1Daito Co., Ltd.
02 1Daiwa Pharmaceutical Industries Co., Ltd.
03 1MEDICHEM, S. A.
04 1Permakem Asia Co., Ltd.
05 1Polaris AI Pharma Corp.
06 1SUN PHARMACEUTICAL INDUSTRIES LTD.
07 1Synthon BV
01 1FLUVOXAMINE MALEATE
02 1Fluvoxamine Maleate
03 4Fluvoxamine maleate
04 1Fluvoxamine maleate (production only)
01 1Gabon
02 2India
03 2Japan
04 1South Korea
05 1Spain
Registration Number : 221MF10066
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2009-03-26
Latest Date of Registration : 2009-03-26
Fluvoxamine Maleate (for manufacturing purposes only)
Registration Number : 221MF10255
Registrant's Address : 2-3-5 Shimookui, Toyama City, Toyama Prefecture
Initial Date of Registration : 2009-11-30
Latest Date of Registration : 2023-11-22
Registration Number : 224MF10206
Registrant's Address : Microweg 22, 6545 CM Nijmegen The Netherlands
Initial Date of Registration : 2012-10-11
Latest Date of Registration : 2012-10-11
Registration Number : 221MF10150
Registrant's Address : 25, Barangongdan-ro, Hyangnam-eup, Hwaseong-si, Gyeonggi-do, Korea
Initial Date of Registration : 2009-07-09
Latest Date of Registration : 2022-10-19
Registration Number : 221MF10116
Registrant's Address : 7-6, Nihonbashi Odenmacho, Chuo-ku, Tokyo
Initial Date of Registration : 2009-06-16
Latest Date of Registration : 2009-06-16
Registration Number : 221MF10042
Registrant's Address : SUN HOUSE, Plot No. 201 B/1, Western Express Highway, Goregaon (E), Mumbai 400063, Ma...
Initial Date of Registration : 2009-02-23
Latest Date of Registration : 2009-02-23
Registration Number : 221MF10111
Registrant's Address : 6-8, Fructo(´)s Gelabert 08970 Sant Joan Despi(´) (Barcelona) Spain
Initial Date of Registration : 2009-06-05
Latest Date of Registration : 2009-06-05
A Fluvoxamine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Fluvoxamine, including repackagers and relabelers. The FDA regulates Fluvoxamine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Fluvoxamine 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 Fluvoxamine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Fluvoxamine supplier is an individual or a company that provides Fluvoxamine active pharmaceutical ingredient (API) or Fluvoxamine finished formulations upon request. The Fluvoxamine suppliers may include Fluvoxamine API manufacturers, exporters, distributors and traders.
click here to find a list of Fluvoxamine 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 Fluvoxamine Drug Master File in Japan (Fluvoxamine JDMF) empowers Fluvoxamine 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 Fluvoxamine JDMF during the approval evaluation for pharmaceutical products. At the time of Fluvoxamine 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 Fluvoxamine suppliers with JDMF on PharmaCompass.
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