01 1FORMOSA LABORATORIES, INC.
02 1Joint Stock Company Grindeks
03 1Shandong New Time Pharmaceutical Co. , Ltd.
01 1Ftorafur
02 2Tegafur
01 1China
02 1Latvia
03 1Taiwan
Registration Number : 224MF10136
Registrant's Address : 36 Hoping Street, Louchu, Taoyuan 33842, Taiwan
Initial Date of Registration : 2012-07-19
Latest Date of Registration : 2012-07-19
Registration Number : 217MF10470
Registrant's Address : 53 Krustpils Street, Riga, Latvia
Initial Date of Registration : 2005-08-24
Latest Date of Registration : 2015-11-19
Registration Number : 304MF10137
Registrant's Address : No. 1, North Outer Ring Road, Feixian County, Shandong Province, China
Initial Date of Registration : 2022-10-05
Latest Date of Registration : 2022-10-05
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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, 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.
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, and COA 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, and COA 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.
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