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
71335-1623-2	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)
70518-1377-0	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1377-0)
70518-1377-1	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190709	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1377-1)
70518-1377-3	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210803	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	100 POUCH in 1 BOX (70518-1377-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-4)
42708-181-60	42708-181	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230804	N/A	ANDA	ANDA077614	QPharma Inc	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (42708-181-60)
50090-4171-0	50090-4171	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-4171-0)
50090-4171-1	50090-4171	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (50090-4171-1)
50090-4171-3	50090-4171	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210924	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-4171-3)
50090-4171-4	50090-4171	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-4171-4)
50090-5726-0	50090-5726	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210928	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5726-0)
51655-029-25	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-25)
51655-029-26	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20221122	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-26)
51655-029-52	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20150209	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-029-52)
51655-030-25	51655-030	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220413	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	12.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-25)
51655-030-26	51655-030	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220714	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	12.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-26)
51655-030-52	51655-030	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220323	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-52)