DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
01 1Dr. Reddy's Laboratories Ltd.
02 1Boryung Corporation
03 1Hetero Labs Limited
04 1Hubei Haosun Pharmaceutical Co. ,Ltd
05 1Jiangsu Xidi Pharmaceuticals Co. , Ltd.
06 1Sanyo Chemical Research Institute Co., Ltd.
01 4Dasatinib
02 1Dasatinib Monohydrate
03 1Dasatinib anhydrous
01 1China
02 1Gabon
03 2India
04 1South Korea
05 1Blank
DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
Registration Number : 304MF10052
Registrant's Address : 8-2-337, Road No. 3, Banjara Hills, Hyderabad 500 034, TELANGANA, INDIA
Initial Date of Registration : 2022-03-10
Latest Date of Registration : 2022-03-10
Registration Number : 303MF10014
Registrant's Address : No. 3 Jiangfeng road, Life and Health Industrial Park, Qidong City 226200, Jiangsu Pr...
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2021-01-26
Registration Number : 303MF10015
Registrant's Address : 136, Changgyeonggung-ro, Jongno-gu, Seoul, Korea
Initial Date of Registration : 2021-01-26
Latest Date of Registration : 2021-01-26
Registration Number : 302MF10086
Registrant's Address : 7-2-A2,Hetero Corporate,Industrial Estates Sanath Nagar,Hyderabad-500 018 Telangana I...
Initial Date of Registration : 2020-07-22
Latest Date of Registration : 2020-07-22
Registration Number : 302MF10139
Registrant's Address : 148-1 Tajii, Mihara-ku, Sakai City, Osaka Prefecture
Initial Date of Registration : 2020-11-26
Latest Date of Registration : 2020-11-26
Registration Number : 306MF10151
Registrant's Address : No. 20 Juxian Road, Gedian Economic & Technology Development Area, Hubei, 436070, P. ...
Initial Date of Registration : 2024-11-27
Latest Date of Registration : 2024-11-27
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A Dasatinib manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Dasatinib, including repackagers and relabelers. The FDA regulates Dasatinib manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Dasatinib 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 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Dasatinib supplier is an individual or a company that provides Dasatinib active pharmaceutical ingredient (API) or Dasatinib finished formulations upon request. The Dasatinib suppliers may include Dasatinib API manufacturers, exporters, distributors and traders.
click here to find a list of Dasatinib 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 Drug Master File in Japan (Dasatinib JDMF) empowers Dasatinib 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 JDMF during the approval evaluation for pharmaceutical products. At the time of Dasatinib 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 suppliers with JDMF on PharmaCompass.
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