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
71335-0273-3	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180702	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0273-3)
71335-0273-4	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180507	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0273-4)
71335-0273-5	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240709	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0273-5)
71335-0273-6	71335-0273	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180213	N/A	ANDA	ANDA078332	Bryant Ranch Prepack	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-0273-6)
43063-125-90	43063-125	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240731	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-125-90)
43063-125-93	43063-125	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20120620	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-125-93)
43063-126-60	43063-126	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20131030	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-126-60)
43063-126-93	43063-126	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20131030	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-126-93)
43063-129-30	43063-129	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140219	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-129-30)
43063-129-60	43063-129	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140219	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-129-60)
43063-129-93	43063-129	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140219	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-129-93)
68071-4600-3	68071-4600	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA078332	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4600-3)
68071-4600-6	68071-4600	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA078332	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-4600-6)
68071-4600-8	68071-4600	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA078332	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (68071-4600-8)
68071-4600-9	68071-4600	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20181017	N/A	ANDA	ANDA078332	NuCare Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-4600-9)
43063-833-60	43063-833	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180201	N/A	ANDA	ANDA078332	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-833-60)