01 1Shizuoka Caffeine Industrial Co., Ltd.
01 1Flufenamic acid aluminum (manufactured only)
01 1Japan
Aluminum flufenamate (for manufacturing purposes only)
Registration Number : 217MF10616
Registrant's Address : 129 Suido-cho, Aoi-ku, Shizuoka City, Shizuoka Prefecture
Initial Date of Registration : 2005-09-14
Latest Date of Registration : 2008-05-29
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PharmaCompass offers a list of Flufenamic Acid 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 Flufenamic Acid manufacturer or Flufenamic Acid supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Flufenamic Acid manufacturer or Flufenamic Acid supplier.
PharmaCompass also assists you with knowing the Flufenamic Acid API Price utilized in the formulation of products. Flufenamic Acid API Price is not always fixed or binding as the Flufenamic Acid Price is obtained through a variety of data sources. The Flufenamic Acid Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Parlif manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Parlif, including repackagers and relabelers. The FDA regulates Parlif manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Parlif 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 Parlif manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Parlif supplier is an individual or a company that provides Parlif active pharmaceutical ingredient (API) or Parlif finished formulations upon request. The Parlif suppliers may include Parlif API manufacturers, exporters, distributors and traders.
click here to find a list of Parlif 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 Parlif Drug Master File in Japan (Parlif JDMF) empowers Parlif 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 Parlif JDMF during the approval evaluation for pharmaceutical products. At the time of Parlif 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 Parlif suppliers with JDMF on PharmaCompass.
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