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01 FORMOSA LABORATORIES, INC. (1)
02 Joint Stock Company Grindeks (1)
03 Sanyo Chemical Research Institute Co., Ltd. (1)
04 Shandong New Time Pharmaceutical Co. , Ltd. (1)
01 Ftorafur (1)
02 Japanese Pharmacopoeia tegafur (production only) (1)
03 Tegafur (2)
01 China (1)
02 Gabon (1)
03 Latvia (1)
04 Taiwan (1)
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PharmaCompass offers a list of Tegafur 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 Tegafur manufacturer or Tegafur supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Tegafur manufacturer or Tegafur supplier.
PharmaCompass also assists you with knowing the Tegafur API Price utilized in the formulation of products. Tegafur API Price is not always fixed or binding as the Tegafur Price is obtained through a variety of data sources. The Tegafur Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Tegafur manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Tegafur, including repackagers and relabelers. The FDA regulates Tegafur manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Tegafur 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 Tegafur manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Tegafur supplier is an individual or a company that provides Tegafur active pharmaceutical ingredient (API) or Tegafur finished formulations upon request. The Tegafur suppliers may include Tegafur API manufacturers, exporters, distributors and traders.
click here to find a list of Tegafur 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 Tegafur Drug Master File in Japan (Tegafur JDMF) empowers Tegafur 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 Tegafur JDMF during the approval evaluation for pharmaceutical products. At the time of Tegafur 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 Tegafur suppliers with JDMF on PharmaCompass.
We have 3 companies offering Tegafur
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