01 1Ajinomoto Co., Inc.
02 1Organic Synthetic Chemicals Industry Co., Ltd.
01 2Trifluridine
01 2Japan
Registration Number : 302MF10048
Registrant's Address : 1-15-1 Kyobashi, Chuo-ku, Tokyo
Initial Date of Registration : 2020-04-17
Latest Date of Registration : 2022-12-07
Registration Number : 225MF10028
Registrant's Address : 3-10-4 Nihonbashi Ningyocho, Chuo-ku, Tokyo
Initial Date of Registration : 2013-02-13
Latest Date of Registration : 2022-10-19
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PharmaCompass offers a list of Trifluridine 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 Trifluridine manufacturer or Trifluridine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Trifluridine manufacturer or Trifluridine supplier.
PharmaCompass also assists you with knowing the Trifluridine API Price utilized in the formulation of products. Trifluridine API Price is not always fixed or binding as the Trifluridine Price is obtained through a variety of data sources. The Trifluridine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A DB00432 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of DB00432, including repackagers and relabelers. The FDA regulates DB00432 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. DB00432 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 DB00432 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A DB00432 supplier is an individual or a company that provides DB00432 active pharmaceutical ingredient (API) or DB00432 finished formulations upon request. The DB00432 suppliers may include DB00432 API manufacturers, exporters, distributors and traders.
click here to find a list of DB00432 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 DB00432 Drug Master File in Japan (DB00432 JDMF) empowers DB00432 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 DB00432 JDMF during the approval evaluation for pharmaceutical products. At the time of DB00432 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 DB00432 suppliers with JDMF on PharmaCompass.
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