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
71335-1545-7	71335-1545	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240430	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	12.5 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-1545-7)
71335-1623-1	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1623-1)
71335-1623-2	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1623-2)
71335-1623-3	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1623-3)
71335-1623-4	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1623-4)
71335-1623-5	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1623-5)
71335-1623-6	71335-1623	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-1623-6)