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
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)
70518-0426-4	70518-0426	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190107	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-0426-4)
70518-4389-0	70518-4389	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250708	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-0)
70518-4389-1	70518-4389	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250819	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	12.5 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-4389-1)
72789-411-90	72789-411	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20240610	N/A	ANDA	ANDA077614	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	3.125 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-411-90)
72789-537-93	72789-537	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20251223	N/A	ANDA	ANDA077614	PD-Rx Pharmaceuticals, Inc.	CARVEDILOL	12.5 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-537-93)
82009-125-05	82009-125	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-125-05)
82009-126-05	82009-126	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-126-05)
82009-127-05	82009-127	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-127-05)
82009-128-05	82009-128	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20230803	N/A	ANDA	ANDA077614	Quallent Pharmaceuticals Health LLC	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-128-05)