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 only)
Registration Number : 218MF10560
Registrant's Address : 1-31 Kannanbecho, Sakai-ku, Sakai-shi, Osaka
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 AK-46307 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of AK-46307, including repackagers and relabelers. The FDA regulates AK-46307 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. AK-46307 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 AK-46307 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A AK-46307 supplier is an individual or a company that provides AK-46307 active pharmaceutical ingredient (API) or AK-46307 finished formulations upon request. The AK-46307 suppliers may include AK-46307 API manufacturers, exporters, distributors and traders.
click here to find a list of AK-46307 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 AK-46307 Drug Master File in Japan (AK-46307 JDMF) empowers AK-46307 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 AK-46307 JDMF during the approval evaluation for pharmaceutical products. At the time of AK-46307 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 AK-46307 suppliers with JDMF on PharmaCompass.
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