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
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)
68788-9789-3	68788-9789	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20120604	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-9789-3)
68788-9789-6	68788-9789	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20120604	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-9789-6)
68788-9789-9	68788-9789	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20120604	N/A	ANDA	ANDA077614	Preferred Pharmaceuticals,Inc.	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-9789-9)