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
80725-141-20	80725-141	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Waylis Therapeutics LLC	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80725-141-20)
80725-142-20	80725-142	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Waylis Therapeutics LLC	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80725-142-20)
80725-140-20	80725-140	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Waylis Therapeutics LLC	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80725-140-20)
80725-139-20	80725-139	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Waylis Therapeutics LLC	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (80725-139-20)
69784-139-20	69784-139	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Woodward Pharma Services LLC	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69784-139-20)
69784-142-20	69784-142	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Woodward Pharma Services LLC	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69784-142-20)
69784-141-20	69784-141	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Woodward Pharma Services LLC	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69784-141-20)
69784-140-20	69784-140	HUMAN PRESCRIPTION DRUG	Coreg	Carvedilol	TABLET, FILM COATED	ORAL	20230415	N/A	NDA	NDA020297	Woodward Pharma Services LLC	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (69784-140-20)