01 1Asahi Kasei Finechem Co., Ltd.
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
Registration Number : 218MF10475
Registrant's Address : 2-10-1 Shinseicho, 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.
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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 04079A1RDZ manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of 04079A1RDZ, including repackagers and relabelers. The FDA regulates 04079A1RDZ manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. 04079A1RDZ 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 04079A1RDZ manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A 04079A1RDZ supplier is an individual or a company that provides 04079A1RDZ active pharmaceutical ingredient (API) or 04079A1RDZ finished formulations upon request. The 04079A1RDZ suppliers may include 04079A1RDZ API manufacturers, exporters, distributors and traders.
click here to find a list of 04079A1RDZ 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 04079A1RDZ Drug Master File in Japan (04079A1RDZ JDMF) empowers 04079A1RDZ 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 04079A1RDZ JDMF during the approval evaluation for pharmaceutical products. At the time of 04079A1RDZ JDMF registration, PMDA checks if the format is accurate, if the necessary items have been included (application), and if data has been attached.
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