01 1FORMOSA LABORATORIES, INC.
02 1Joint Stock Company Grindeks
03 1Sanyo Chemical Research Institute Co., Ltd.
04 1Shandong New Time Pharmaceutical Co. , Ltd.
01 1Ftorafur
02 1Japanese Pharmacopoeia tegafur (production only)
03 2Tegafur
01 1China
02 1Gabon
03 1Latvia
04 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
Japanese Pharmacopoeia Tegafur (for manufacturing only)
Registration Number : 217MF10160
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2005-05-31
Latest Date of Registration : 2006-11-15
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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 Lifril manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Lifril, including repackagers and relabelers. The FDA regulates Lifril manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Lifril 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 Lifril manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Lifril supplier is an individual or a company that provides Lifril active pharmaceutical ingredient (API) or Lifril finished formulations upon request. The Lifril suppliers may include Lifril API manufacturers, exporters, distributors and traders.
click here to find a list of Lifril 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 Lifril Drug Master File in Japan (Lifril JDMF) empowers Lifril 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 Lifril JDMF during the approval evaluation for pharmaceutical products. At the time of Lifril 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 Lifril suppliers with JDMF on PharmaCompass.
We have 3 companies offering Lifril
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