DRL offers a portfolio of products & services, including APIs, CMO services, generics, biosimilars & differentiated formulations.
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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.
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01 3Dasatinib
02 1Dasatinib Monohydrate
03 1Dasatinib anhydrous
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01 2China
02 2India
03 1South Korea
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 : 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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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.
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A Sprycel (Bristol Meyers) manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Sprycel (Bristol Meyers), including repackagers and relabelers. The FDA regulates Sprycel (Bristol Meyers) manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Sprycel (Bristol Meyers) API Manufacturers are required to adhere to Good Manufacturing Practices (GMP) to ensure that their products are consistently manufactured to meet established quality criteria.
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A Sprycel (Bristol Meyers) supplier is an individual or a company that provides Sprycel (Bristol Meyers) active pharmaceutical ingredient (API) or Sprycel (Bristol Meyers) finished formulations upon request. The Sprycel (Bristol Meyers) suppliers may include Sprycel (Bristol Meyers) API manufacturers, exporters, distributors and traders.
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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 Sprycel (Bristol Meyers) Drug Master File in Japan (Sprycel (Bristol Meyers) JDMF) empowers Sprycel (Bristol Meyers) 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 Sprycel (Bristol Meyers) JDMF during the approval evaluation for pharmaceutical products. At the time of Sprycel (Bristol Meyers) 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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