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
71335-2033-4	71335-2033	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA078165	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (71335-2033-4)
71335-2033-5	71335-2033	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA078165	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2033-5)
71335-2033-6	71335-2033	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA078165	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-2033-6)
71335-2033-7	71335-2033	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA078165	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	25 TABLET, FILM COATED in 1 BOTTLE (71335-2033-7)
71335-2033-8	71335-2033	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA078165	Bryant Ranch Prepack	CARVEDILOL	6.25 mg/1	10 TABLET, FILM COATED in 1 BOTTLE (71335-2033-8)
70518-3524-0	70518-3524	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20220917	N/A	ANDA	ANDA078165	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-3524-0)
70518-3524-1	70518-3524	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20230128	N/A	ANDA	ANDA078165	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3524-1)
70518-3524-2	70518-3524	HUMAN PRESCRIPTION DRUG	CARVEDILOL	CARVEDILOL	TABLET, FILM COATED	ORAL	20230210	N/A	ANDA	ANDA078165	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-3524-2)