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
68071-2633-6	68071-2633	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220201	N/A	ANDA	ANDA078384	NuCare Pharmaceuticals,Inc.	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2633-6)
68071-2633-8	68071-2633	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220201	N/A	ANDA	ANDA078384	NuCare Pharmaceuticals,Inc.	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2633-8)
68071-2633-9	68071-2633	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220201	N/A	ANDA	ANDA078384	NuCare Pharmaceuticals,Inc.	CARVEDILOL	3.125 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2633-9)
71335-1813-1	71335-1813	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220214	N/A	ANDA	ANDA078384	Bryant Ranch Prepack	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71335-1813-1)
51407-039-05	51407-039	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA078384	Golden State Medical Supply, Inc.	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-039-05)
51407-039-01	51407-039	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA078384	Golden State Medical Supply, Inc.	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51407-039-01)
76385-110-01	76385-110	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-110-01)
76385-112-01	76385-112	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-112-01)
76385-112-50	76385-112	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-112-50)
76385-113-01	76385-113	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-113-01)
76385-113-50	76385-113	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-113-50)
51655-713-25	51655-713	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220415	N/A	ANDA	ANDA078384	Northwind Pharmaceuticals	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-25)
51655-713-52	51655-713	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210528	N/A	ANDA	ANDA078384	Northwind Pharmaceuticals	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-713-52)
51655-943-18	51655-943	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220330	N/A	ANDA	ANDA078384	Northwind Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-943-18)
76385-110-50	76385-110	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-110-50)
76385-111-01	76385-111	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-111-01)
76385-111-50	76385-111	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20161001	N/A	ANDA	ANDA078384	Bayshore Pharmaceuticals LLC	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (76385-111-50)