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
0781-5221-01	0781-5221	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	20260630	ANDA	ANDA078227	Sandoz Inc	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5221-01)
72189-372-30	72189-372	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220810	N/A	ANDA	ANDA078227	Direct_Rx	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-372-30)
0781-5222-01	0781-5222	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	20260430	ANDA	ANDA078227	Sandoz Inc	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5222-01)
0781-5223-01	0781-5223	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	20260831	ANDA	ANDA078227	Sandoz Inc	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5223-01)
0781-5224-01	0781-5224	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	20260831	ANDA	ANDA078227	Sandoz Inc	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0781-5224-01)