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
68382-092-17	68382-092	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Pharmaceuticals USA Inc.	CARVEDILOL	3.125 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (68382-092-17)
70518-0356-0	70518-0356	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20170323	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0356-0)
70518-0356-1	70518-0356	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20171016	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0356-1)
68001-153-00	68001-153	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-153-00)
68001-153-03	68001-153	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68001-153-03)
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)
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)
68788-9265-1	68788-9265	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141203	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals,Inc.	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-9265-1)
65841-618-01	65841-618	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-618-01)
65841-618-05	65841-618	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-618-05)
65841-618-17	65841-618	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	12.5 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-618-17)
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)
68071-2230-6	68071-2230	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20200804	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	12.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-2230-6)