01 Dr. Reddy's Laboratories Ltd. (1)
02 Boryung Corporation (1)
03 Hetero Labs Limited (1)
04 Jiangsu Xidi Pharmaceuticals Co., Ltd. (1)
05 Sanyo Chemical Research Institute Co., Ltd. (1)
01 Dasatinib (4)
02 Dasatinib Monohydrate (1)
01 China (1)
02 Gabon (1)
03 India (2)
04 South Korea (1)
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PharmaCompass offers a list of Dasatinib 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 Dasatinib manufacturer or Dasatinib supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Dasatinib manufacturer or Dasatinib supplier.
PharmaCompass also assists you with knowing the Dasatinib API Price utilized in the formulation of products. Dasatinib API Price is not always fixed or binding as the Dasatinib Price is obtained through a variety of data sources. The Dasatinib Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Dasatinib (anhydrous) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dasatinib (anhydrous), including repackagers and relabelers. The FDA regulates Dasatinib (anhydrous) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dasatinib (anhydrous) 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 Dasatinib (anhydrous) manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dasatinib (anhydrous) supplier is an individual or a company that provides Dasatinib (anhydrous) active pharmaceutical ingredient (API) or Dasatinib (anhydrous) finished formulations upon request. The Dasatinib (anhydrous) suppliers may include Dasatinib (anhydrous) API manufacturers, exporters, distributors and traders.
click here to find a list of Dasatinib (anhydrous) 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 Dasatinib (anhydrous) Drug Master File in Japan (Dasatinib (anhydrous) JDMF) empowers Dasatinib (anhydrous) 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 Dasatinib (anhydrous) JDMF during the approval evaluation for pharmaceutical products. At the time of Dasatinib (anhydrous) 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 Dasatinib (anhydrous) suppliers with JDMF on PharmaCompass.
We have 4 companies offering Dasatinib (anhydrous)
Get in contact with the supplier of your choice: