01 1Nantong Chanyoo Pharmatech Co. ,Ltd
02 1Shanghai Desano Chemical Pharmaceutical Co. , Ltd.
03 1Shiratori Pharmaceutical Co., Ltd.
04 1Sichuan D-Innovation Pharmaceutical Co. , Ltd.
01 3Eltrombopag Olamine
02 1Eltrombopag Olamine Manufacturing Only
01 3China
02 1Japan
Registration Number : 307MF10019
Registrant's Address : #2 Tonghai Si Rd Yangkou Chemical Industrial Park Rudong Coastal Economic Development...
Initial Date of Registration : 2025-01-23
Latest Date of Registration : 2025-01-23
Registration Number : 307MF10017
Registrant's Address : No. 1479, Zhangjiang Road, Zhangjiang High Tech Park, Shanghai 201203, China
Initial Date of Registration : 2025-01-23
Latest Date of Registration : 2025-11-13
Eltrombopag Olamine For manufacturing purposes only
Registration Number : 307MF10029
Registrant's Address : 6-11-24 Tsudanuma, Narashino City, Chiba Prefecture
Initial Date of Registration : 2025-02-07
Latest Date of Registration : 2025-02-07
Registration Number : 307MF10077
Registrant's Address : No. 13, Yulan Road, Western Medical Valley, New Zone, Economic Development Zone, Meis...
Initial Date of Registration : 2025-07-03
Latest Date of Registration : 2025-07-03
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PharmaCompass offers a list of Eltrombopag 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 Eltrombopag manufacturer or Eltrombopag supplier for your needs.
Send us enquiries for free, and we will assist you in establishing a direct connection with your preferred Eltrombopag manufacturer or Eltrombopag supplier.
PharmaCompass also assists you with knowing the Eltrombopag API Price utilized in the formulation of products. Eltrombopag API Price is not always fixed or binding as the Eltrombopag Price is obtained through a variety of data sources. The Eltrombopag Price can also vary due to multiple factors, including market conditions, regulatory modifications, or negotiated pricing deals.
A Revolade manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of Revolade, including repackagers and relabelers. The FDA regulates Revolade manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. Revolade 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 Revolade manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A Revolade supplier is an individual or a company that provides Revolade active pharmaceutical ingredient (API) or Revolade finished formulations upon request. The Revolade suppliers may include Revolade API manufacturers, exporters, distributors and traders.
click here to find a list of Revolade 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 Revolade Drug Master File in Japan (Revolade JDMF) empowers Revolade 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 Revolade JDMF during the approval evaluation for pharmaceutical products. At the time of Revolade 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 Revolade suppliers with JDMF on PharmaCompass.
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