01 1Shizuoka Caffeine Industry Co., Ltd.
01 1Flufenamic acid aluminum (manufactured only)
01 1Japan
Aluminum flufenamate (for manufacturing only)
Registration Number : 217MF10616
Registrant's Address : 129 Suidocho, Aoi Ward, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2008-05-29
A Flufenamic Acid manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Flufenamic Acid, including repackagers and relabelers. The FDA regulates Flufenamic Acid manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Flufenamic Acid 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 Flufenamic Acid manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Flufenamic Acid supplier is an individual or a company that provides Flufenamic Acid active pharmaceutical ingredient (API) or Flufenamic Acid finished formulations upon request. The Flufenamic Acid suppliers may include Flufenamic Acid API manufacturers, exporters, distributors and traders.
click here to find a list of Flufenamic Acid 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 Flufenamic Acid Drug Master File in Japan (Flufenamic Acid JDMF) empowers Flufenamic Acid 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 Flufenamic Acid JDMF during the approval evaluation for pharmaceutical products. At the time of Flufenamic Acid 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 Flufenamic Acid suppliers with JDMF on PharmaCompass.
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