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
63304-097-13	63304-097	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	25 mg/1	120 TABLET in 1 BOTTLE (63304-097-13)
63304-097-19	63304-097	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	25 mg/1	1 BLISTER PACK in 1 CARTON (63304-097-19) / 9 TABLET in 1 BLISTER PACK
63304-097-45	63304-097	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	25 mg/1	5 TABLET in 1 BOTTLE (63304-097-45)
63304-098-13	63304-098	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	50 mg/1	120 TABLET in 1 BOTTLE (63304-098-13)
63304-098-19	63304-098	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	50 mg/1	1 BLISTER PACK in 1 CARTON (63304-098-19) / 9 TABLET in 1 BLISTER PACK
63304-098-45	63304-098	HUMAN PRESCRIPTION DRUG	Sumatriptan	Sumatriptan	TABLET	ORAL	20090813	N/A	ANDA	ANDA076554	SUN PHARMACEUTICAL INDUSTRIES, INC.	SUMATRIPTAN SUCCINATE	50 mg/1	5 TABLET in 1 BOTTLE (63304-098-45)
63187-164-09	63187-164	HUMAN PRESCRIPTION DRUG	SUMATRIPTAN	SUMATRIPTAN	TABLET	ORAL	20190101	N/A	ANDA	ANDA076554	Proficient Rx LP	SUMATRIPTAN SUCCINATE	25 mg/1	9 TABLET in 1 BLISTER PACK (63187-164-09)