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
65841-619-17	65841-619	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	25 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (65841-619-17)
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)
65841-617-01	65841-617	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070905	N/A	ANDA	ANDA077614	Zydus Lifesciences Limited	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (65841-617-01)
68001-151-00	68001-151	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-151-00)
68001-151-03	68001-151	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68001-151-03)
68001-152-00	68001-152	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-152-00)
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)
68001-154-03	68001-154	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68001-154-03)
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)
68001-154-00	68001-154	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68001-154-00)
68001-152-03	68001-152	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140422	N/A	ANDA	ANDA077614	BluePoint Laboratories	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68001-152-03)
68071-2230-3	68071-2230	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250102	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-2230-3)
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)
68084-854-01	68084-854	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20150504	N/A	ANDA	ANDA077614	American Health Packaging	CARVEDILOL	6.25 mg/1	100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-854-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-854-11)
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)
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)