01 1Asahi Kasei Finechem Corporation
02 1Yamasa Soy Sauce Co., Ltd.
01 1Cytarabine ocfosfate "Yamasa"
02 1Japanese Pharmacopoeia cytarabine (production only)
01 2Japan
Japanese Pharmacopoeia Cytarabine (for manufacturing purposes only)
Registration Number : 217MF10811
Registrant's Address : 3-3-23 Nakanoshima, Kita-ku, Osaka City, Osaka Prefecture
Initial Date of Registration : 2005-11-01
Latest Date of Registration : 2007-08-01
Cytarabine ocphosphonate "Yamasa"
Registration Number : 218MF10475
Registrant's Address : 2-10-1 Shinsei-cho, Choshi City, Chiba Prefecture
Initial Date of Registration : 2006-05-15
Latest Date of Registration : 2009-01-28
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PharmaCompass offers a list of Cytarabine 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 Cytarabine manufacturer or Cytarabine supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Cytarabine manufacturer or Cytarabine supplier.
PharmaCompass also assists you with knowing the Cytarabine API Price utilized in the formulation of products. Cytarabine API Price is not always fixed or binding as the Cytarabine Price is obtained through a variety of data sources. The Cytarabine Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Cytosar manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytosar, including repackagers and relabelers. The FDA regulates Cytosar manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytosar 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 Cytosar manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytosar supplier is an individual or a company that provides Cytosar active pharmaceutical ingredient (API) or Cytosar finished formulations upon request. The Cytosar suppliers may include Cytosar API manufacturers, exporters, distributors and traders.
click here to find a list of Cytosar 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 Cytosar Drug Master File in Japan (Cytosar JDMF) empowers Cytosar 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 Cytosar JDMF during the approval evaluation for pharmaceutical products. At the time of Cytosar 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 Cytosar suppliers with JDMF on PharmaCompass.
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