01 1Sanbo Chemical Laboratory Co., Ltd.
02 1Sicor de Me(´)xico,S. A. de C. V.
01 1Fluorouracil "Teva 2"
02 1Japanese Pharmacopoeia fluorouracil (production only)
01 1Japan
02 1Mexico
Japanese Pharmacopoeia Fluorouracil (for manufacturing purposes only)
Registration Number : 218MF10560
Registrant's Address : 1-31 Kannanbecho, Sakai Ward, Sakai City, Osaka Prefecture
Initial Date of Registration : 2006-06-02
Latest Date of Registration : 2006-09-22
Registration Number : 227MF10172
Registrant's Address : Av. San Rafael No. 35 Parque Industrial Lerma, CP52000 Lerma, Edo. Me(´)xico. MEXICO
Initial Date of Registration : 2015-06-26
Latest Date of Registration : 2015-06-26
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PharmaCompass offers a list of Fluorouracil 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 Fluorouracil manufacturer or Fluorouracil supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Fluorouracil manufacturer or Fluorouracil supplier.
PharmaCompass also assists you with knowing the Fluorouracil API Price utilized in the formulation of products. Fluorouracil API Price is not always fixed or binding as the Fluorouracil Price is obtained through a variety of data sources. The Fluorouracil Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A URF manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of URF, including repackagers and relabelers. The FDA regulates URF manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. URF 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 URF manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A URF supplier is an individual or a company that provides URF active pharmaceutical ingredient (API) or URF finished formulations upon request. The URF suppliers may include URF API manufacturers, exporters, distributors and traders.
click here to find a list of URF 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 URF Drug Master File in Japan (URF JDMF) empowers URF 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 URF JDMF during the approval evaluation for pharmaceutical products. At the time of URF 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 URF suppliers with JDMF on PharmaCompass.
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