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 purposes 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
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PharmaCompass offers a list of Flavoxate API manufacturers, exporters & distributors, which can be sorted by GMP, USDMF, JDMF, KDMF, CEP (COS), WC, Price,and more, enabling you to easily find the right Flavoxate manufacturer or Flavoxate supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flavoxate manufacturer or Flavoxate supplier.
PharmaCompass also assists you with knowing the Flavoxate API Price utilized in the formulation of products. Flavoxate API Price is not always fixed or binding as the Flavoxate Price is obtained through a variety of data sources. The Flavoxate Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Uronid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Uronid, including repackagers and relabelers. The FDA regulates Uronid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Uronid 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 Uronid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Uronid supplier is an individual or a company that provides Uronid active pharmaceutical ingredient (API) or Uronid finished formulations upon request. The Uronid suppliers may include Uronid API manufacturers, exporters, distributors and traders.
click here to find a list of Uronid 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 Uronid Drug Master File in Japan (Uronid JDMF) empowers Uronid 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 Uronid JDMF during the approval evaluation for pharmaceutical products. At the time of Uronid 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 Uronid suppliers with JDMF on PharmaCompass.
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