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
65862-142-99	65862-142	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	3.125 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-142-99)
65862-143-01	65862-143	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-143-01)
65862-143-99	65862-143	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	6.25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-143-99)
65862-145-01	65862-145	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-145-01)
65862-145-05	65862-145	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-145-05)
65862-145-99	65862-145	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-145-99)
65862-144-01	65862-144	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65862-144-01)
65862-144-05	65862-144	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65862-144-05)
65862-144-99	65862-144	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA078332	Aurobindo Pharma Limited	CARVEDILOL	12.5 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (65862-144-99)
71335-0273-1	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230906	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-0273-1)
71335-0273-5	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0273-5)
71335-0273-6	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180213	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0273-6)
71335-0273-7	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-0273-7)
71335-0273-2	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180330	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0273-2)
71335-0273-3	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0273-3)
71335-0273-4	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180507	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0273-4)