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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 Cytarabine manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Cytarabine, including repackagers and relabelers. The FDA regulates Cytarabine manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Cytarabine 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 Cytarabine manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Cytarabine supplier is an individual or a company that provides Cytarabine active pharmaceutical ingredient (API) or Cytarabine finished formulations upon request. The Cytarabine suppliers may include Cytarabine API manufacturers, exporters, distributors and traders.
click here to find a list of Cytarabine 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 Cytarabine Drug Master File in Japan (Cytarabine JDMF) empowers Cytarabine 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 Cytarabine JDMF during the approval evaluation for pharmaceutical products. At the time of Cytarabine 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 Cytarabine suppliers with JDMF on PharmaCompass.
We have 2 companies offering Cytarabine
Get in contact with the supplier of your choice: