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
0078-0687-15	0078-0687	HUMAN PRESCRIPTION DRUG	PROMACTA	eltrombopag olamine	TABLET, FILM COATED	ORAL	20160401	N/A	NDA	NDA022291	Novartis Pharmaceuticals Corporation	ELTROMBOPAG OLAMINE	75 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0687-15)
0078-0685-15	0078-0685	HUMAN PRESCRIPTION DRUG	PROMACTA	eltrombopag olamine	TABLET, FILM COATED	ORAL	20160524	N/A	NDA	NDA022291	Novartis Pharmaceuticals Corporation	ELTROMBOPAG OLAMINE	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0685-15)
0078-0684-15	0078-0684	HUMAN PRESCRIPTION DRUG	PROMACTA	eltrombopag olamine	TABLET, FILM COATED	ORAL	20160822	N/A	NDA	NDA022291	Novartis Pharmaceuticals Corporation	ELTROMBOPAG OLAMINE	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0684-15)
0078-0686-15	0078-0686	HUMAN PRESCRIPTION DRUG	PROMACTA	eltrombopag olamine	TABLET, FILM COATED	ORAL	20160407	N/A	NDA	NDA022291	Novartis Pharmaceuticals Corporation	ELTROMBOPAG OLAMINE	50 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (0078-0686-15)
0078-0686-55	0078-0686	HUMAN PRESCRIPTION DRUG	PROMACTA	eltrombopag olamine	TABLET, FILM COATED	ORAL	20200121	N/A	NDA	NDA022291	Novartis Pharmaceuticals Corporation	ELTROMBOPAG OLAMINE	50 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (0078-0686-55)