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
60219-1649-3	60219-1649	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	.25 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1649-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
60219-1650-3	60219-1650	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	.5 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1650-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
60219-1651-3	60219-1651	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	1 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1651-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
60219-1652-3	60219-1652	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	2 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1652-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
60219-1653-3	60219-1653	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	3 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1653-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC
60219-1654-3	60219-1654	HUMAN PRESCRIPTION DRUG	brexpiprazole	brexpiprazole	TABLET, FILM COATED	ORAL	20230207	N/A	ANDA	ANDA213562	Amneal Pharmaceuticals NY LLC	BREXPIPRAZOLE	4 mg/1	1 BOTTLE, PLASTIC in 1 CARTON (60219-1654-3) / 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC