美国药品NDC（国家药品编码）与药品说明书数据库（U.S. FDA National Drug Code DataBase）

NDC包装代码	产品NDC	产品类型	商品名	通用名	剂型	给药途径	上市日期	结束日期	市场类别	申请号	标签持有者	活性成分	规格	包装描述
70069-840-01	70069-840	HUMAN PRESCRIPTION DRUG	Eltrombopag olamine	Eltrombopag olamine	TABLET, FILM COATED	ORAL	20260114	N/A	ANDA	ANDA219638	Somerset Therapeutics, LLC	ELTROMBOPAG OLAMINE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70069-840-01)
70069-839-01	70069-839	HUMAN PRESCRIPTION DRUG	Eltrombopag olamine	Eltrombopag olamine	TABLET, FILM COATED	ORAL	20260114	N/A	ANDA	ANDA219638	Somerset Therapeutics, LLC	ELTROMBOPAG OLAMINE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70069-839-01)
70069-838-01	70069-838	HUMAN PRESCRIPTION DRUG	Eltrombopag olamine	Eltrombopag olamine	TABLET, FILM COATED	ORAL	20260114	N/A	ANDA	ANDA219638	Somerset Therapeutics, LLC	ELTROMBOPAG OLAMINE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70069-838-01)
70069-837-01	70069-837	HUMAN PRESCRIPTION DRUG	Eltrombopag olamine	Eltrombopag olamine	TABLET, FILM COATED	ORAL	20260114	N/A	ANDA	ANDA219638	Somerset Therapeutics, LLC	ELTROMBOPAG OLAMINE	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (70069-837-01)