01 1Daito Co., Ltd.
02 2Yamamoto Chemical Industry Co., Ltd.
01 1Day stations flavoxate hydrochloride (production only)
02 1Japanese Pharmacopoeia flavoxate
03 1Japanese Pharmacopoeia flavoxate hydrochloride
01 3Japan
JP Flavoxate Hydrochloride (for manufacturing only)
Registration Number : 218MF10835
Registrant's Address : 326 Yokamachi, Toyama City, Toyama Prefecture
Initial Date of Registration : 2006-10-20
Latest Date of Registration : 2013-04-05
Japanese Pharmacopoeia Flavoxate Hydrochloride
Registration Number : 217MF10560
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2005-09-09
Latest Date of Registration : 2007-05-30
Japanese Pharmacopoeia Flavoxate Hydrochloride
Registration Number : 227MF10194
Registrant's Address : 1-4 Funatsucho, Wakayama City, Wakayama Prefecture
Initial Date of Registration : 2015-08-03
Latest Date of Registration : 2015-08-03
A Flavoxate manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flavoxate, including repackagers and relabelers. The FDA regulates Flavoxate manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flavoxate 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 Flavoxate manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flavoxate supplier is an individual or a company that provides Flavoxate active pharmaceutical ingredient (API) or Flavoxate finished formulations upon request. The Flavoxate suppliers may include Flavoxate API manufacturers, exporters, distributors and traders.
click here to find a list of Flavoxate 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 Flavoxate Drug Master File in Japan (Flavoxate JDMF) empowers Flavoxate 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 Flavoxate JDMF during the approval evaluation for pharmaceutical products. At the time of Flavoxate 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 Flavoxate suppliers with JDMF on PharmaCompass.
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