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
0615-8389-39	0615-8389	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210219	N/A	ANDA	ANDA076373	NCS HealthCare of KY, LLC dba Vangard Labs	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8389-39)
82804-191-60	82804-191	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250201	N/A	ANDA	ANDA076373	Proficient Rx LP	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (82804-191-60)
82804-225-90	82804-225	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250522	N/A	ANDA	ANDA076373	Proficient Rx LP	CARVEDILOL	12.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-225-90)
0615-8390-39	0615-8390	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210211	N/A	ANDA	ANDA076373	NCS HealthCare of KY, LLC dba Vangard Labs	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8390-39)
42708-072-60	42708-072	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180418	N/A	ANDA	ANDA076373	QPharma, Inc.	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (42708-072-60)
0615-8387-05	0615-8387	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230808	N/A	ANDA	ANDA076373	NCS HealthCare of KY, LLC dba Vangard Labs	CARVEDILOL	3.125 mg/1	15 TABLET, FILM COATED in 1 BLISTER PACK (0615-8387-05)
0615-8387-39	0615-8387	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210223	N/A	ANDA	ANDA076373	NCS HealthCare of KY, LLC dba Vangard Labs	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8387-39)
0093-7295-01	0093-7295	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070906	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-7295-01)
0093-7295-05	0093-7295	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20081202	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-7295-05)
0093-0051-01	0093-0051	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070906	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-0051-01)
0093-0051-05	0093-0051	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20081202	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-0051-05)
0615-8388-39	0615-8388	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20210216	N/A	ANDA	ANDA076373	NCS HealthCare of KY, LLC dba Vangard Labs	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8388-39)
0093-7296-01	0093-7296	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070906	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-7296-01)
0093-7296-05	0093-7296	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20081202	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-7296-05)
82804-138-90	82804-138	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240906	N/A	ANDA	ANDA076373	Proficient Rx LP	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (82804-138-90)
0093-0135-01	0093-0135	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20070906	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (0093-0135-01)
0093-0135-05	0093-0135	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20081202	N/A	ANDA	ANDA076373	Teva Pharmaceuticals USA, Inc.	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (0093-0135-05)