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
62756-522-18	62756-522	HUMAN PRESCRIPTION DRUG	sumatriptan succinate	sumatriptan succinate	TABLET, FILM COATED	ORAL	20090810	N/A	ANDA	ANDA078295	Sun Pharmaceutical Industries, Inc.	SUMATRIPTAN SUCCINATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62756-522-18)
62756-522-69	62756-522	HUMAN PRESCRIPTION DRUG	sumatriptan succinate	sumatriptan succinate	TABLET, FILM COATED	ORAL	20090810	N/A	ANDA	ANDA078295	Sun Pharmaceutical Industries, Inc.	SUMATRIPTAN SUCCINATE	100 mg/1	9 BLISTER PACK in 1 CARTON (62756-522-69) / 1 TABLET, FILM COATED in 1 BLISTER PACK
62756-522-83	62756-522	HUMAN PRESCRIPTION DRUG	sumatriptan succinate	sumatriptan succinate	TABLET, FILM COATED	ORAL	20090810	N/A	ANDA	ANDA078295	Sun Pharmaceutical Industries, Inc.	SUMATRIPTAN SUCCINATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62756-522-83)
62756-522-88	62756-522	HUMAN PRESCRIPTION DRUG	sumatriptan succinate	sumatriptan succinate	TABLET, FILM COATED	ORAL	20090810	N/A	ANDA	ANDA078295	Sun Pharmaceutical Industries, Inc.	SUMATRIPTAN SUCCINATE	100 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62756-522-88)
62756-522-93	62756-522	HUMAN PRESCRIPTION DRUG	sumatriptan succinate	sumatriptan succinate	TABLET, FILM COATED	ORAL	20090810	N/A	ANDA	ANDA078295	Sun Pharmaceutical Industries, Inc.	SUMATRIPTAN SUCCINATE	100 mg/1	9 BLISTER PACK in 1 CARTON (62756-522-93) / 1 TABLET, FILM COATED in 1 BLISTER PACK
72189-432-09	72189-432	HUMAN PRESCRIPTION DRUG	Sumatriptan Succinate	Sumatriptan Succinate	TABLET, FILM COATED	ORAL	20230313	N/A	ANDA	ANDA078295	Direct_Rx	SUMATRIPTAN SUCCINATE	25 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (72189-432-09)