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
58657-750-01	58657-750	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-750-01)
58657-750-50	58657-750	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	3.125 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-750-50)
58657-753-01	58657-753	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-753-01)
58657-753-50	58657-753	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-753-50)
58657-752-01	58657-752	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	12.5 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-752-01)
58657-752-50	58657-752	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	12.5 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-752-50)
58657-751-01	58657-751	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-751-01)
58657-751-50	58657-751	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20241203	N/A	ANDA	ANDA078786	Method Pharmaceuticals, LLC	CARVEDILOL	6.25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (58657-751-50)