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
71335-1623-6	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)
71335-2101-1	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2101-1)
71335-2101-2	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220714	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-2101-2)
71335-2101-3	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220721	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-2101-3)
71335-2101-4	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20231117	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2101-4)
71335-2101-5	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240212	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2101-5)
71335-2101-6	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220708	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2101-6)
71335-2101-7	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	25 TABLET, FILM COATED in 1 BOTTLE (71335-2101-7)
71335-2101-8	71335-2101	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2101-8)
72189-663-90	72189-663	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20260302	N/A	ANDA	ANDA077614	Direct_Rx	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-663-90)
72189-664-60	72189-664	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20260305	N/A	ANDA	ANDA077614	Direct_Rx	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-664-60)
82009-125-05	82009-125	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-125-05)
82009-126-05	82009-126	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-126-05)
82009-127-05	82009-127	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-127-05)
82009-128-05	82009-128	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-128-05)