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
0173-0517-00	0173-0517	HUMAN PRESCRIPTION DRUG	FLOLAN	epoprostenol sodium	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	19951208	N/A	NDA	NDA020444	GlaxoSmithKline LLC	EPOPROSTENOL SODIUM	.5 mg/1	1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0517-00)
0173-0857-02	0173-0857	HUMAN PRESCRIPTION DRUG	Diluent	water	SOLUTION	INTRAVENOUS	20160401	N/A	NDA	NDA020444	GlaxoSmithKline LLC	WATER	1 mL/mL	2 VIAL in 1 TRAY (0173-0857-02) / 50 mL in 1 VIAL
0173-0519-00	0173-0519	HUMAN PRESCRIPTION DRUG	FLOLAN	epoprostenol sodium	INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION	INTRAVENOUS	19951208	N/A	NDA	NDA020444	GlaxoSmithKline LLC	EPOPROSTENOL SODIUM	1.5 mg/1	1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 CARTON (0173-0519-00)