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
63187-570-60	63187-570	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077614	Proficient Rx LP	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-570-60)
63187-570-90	63187-570	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181201	N/A	ANDA	ANDA077614	Proficient Rx LP	CARVEDILOL	3.125 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-570-90)
68071-4956-6	68071-4956	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190703	N/A	ANDA	ANDA077614	NuCare Pharmaceuticals,Inc.	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-4956-6)
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)
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)
68001-152-03	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)
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)
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)
68001-154-03	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)
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)
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)
70518-0426-0	70518-0426	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20170417	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0426-0)
70518-0426-1	70518-0426	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20170424	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0426-1)