01 1Nantong Chanyoo Pharmatech Co. ,Ltd
02 1Shanghai Desano Chemical Pharmaceutical Co. , Ltd.
03 1Shiratori Pharmaceutical Co., Ltd.
01 2Eltrombopag Olamine
02 1Eltrombopag Olamine Manufacturing Only
01 2China
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, Zhangheng Road, Zhangjiang High Tech Park, Shanghai 201203, China
Initial Date of Registration : 2025-01-23
Latest Date of Registration : 2025-01-23
Eltrombopag Olamine Manufacturing 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
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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 SB19102 manufacturer is defined as any person or entity involved in the manufacture, preparation, processing, compounding or propagation of SB19102, including repackagers and relabelers. The FDA regulates SB19102 manufacturers to ensure that their products comply with relevant laws and regulations and are safe and effective to use. SB19102 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 SB19102 manufacturers with USDMF, JDMF, KDMF, CEP, GMP, COA and API Price related information on PhamaCompass.
A SB19102 supplier is an individual or a company that provides SB19102 active pharmaceutical ingredient (API) or SB19102 finished formulations upon request. The SB19102 suppliers may include SB19102 API manufacturers, exporters, distributors and traders.
click here to find a list of SB19102 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 SB19102 Drug Master File in Japan (SB19102 JDMF) empowers SB19102 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 SB19102 JDMF during the approval evaluation for pharmaceutical products. At the time of SB19102 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 SB19102 suppliers with JDMF on PharmaCompass.
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