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
70518-1826-1	70518-1826	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190313	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1826-1)
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)
51655-034-25	51655-034	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20221018	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-25)
68788-7539-1	68788-7539	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-7539-1)
68788-7539-3	68788-7539	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-7539-3)
68788-7539-6	68788-7539	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-7539-6)
68788-7539-9	68788-7539	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20191227	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-7539-9)
65841-616-01	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-616-01)
65841-616-05	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (65841-616-05)
65841-616-17	65841-616	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	3.125 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-616-17)
51655-034-52	51655-034	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220809	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-52)
51655-034-83	51655-034	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230111	N/A	ANDA	ANDA077614	Northwind Pharmaceuticals, LLC	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-034-83)
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)
68071-2230-8	68071-2230	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20200804	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-8)
68071-2230-9	68071-2230	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20200804	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	12.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2230-9)
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)
68071-2780-6	68071-2780	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240628	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-2780-6)
68071-2780-8	68071-2780	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220705	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-2780-8)
68071-2780-9	68071-2780	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220705	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2780-9)
50090-1062-0	50090-1062	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141128	N/A	ANDA	ANDA077614	A-S Medication Solutions	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (50090-1062-0)