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
70518-0426-4	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)
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)
70518-0840-2	70518-0840	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20260427	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	6.25 mg/1	50 POUCH in 1 BOX (70518-0840-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-0840-3)
70518-1377-0	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20180815	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1377-0)
70518-1377-1	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190709	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1377-1)
70518-1377-5	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20250514	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	100 POUCH in 1 BOX (70518-1377-5) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6)
70518-1377-7	70518-1377	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20260424	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	3.125 mg/1	50 POUCH in 1 BOX (70518-1377-7) / 1 TABLET, FILM COATED in 1 POUCH (70518-1377-6)
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)
63629-4060-1	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20090827	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-4060-1)
63629-4060-2	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20090904	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (63629-4060-2)
63629-4060-3	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20151124	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	180 TABLET, FILM COATED in 1 BOTTLE (63629-4060-3)
63629-4060-4	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20110502	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-4060-4)
63629-4060-5	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20140530	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-4060-5)
63629-4060-6	63629-4060	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20141028	N/A	ANDA	ANDA077614	Bryant Ranch Prepack	CARVEDILOL	3.125 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (63629-4060-6)
70518-1826-0	70518-1826	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190126	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	25 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1826-0)
70518-1826-1	70518-1826	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20190313	N/A	ANDA	ANDA077614	REMEDYREPACK INC.	CARVEDILOL	25 mg/1	180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1826-1)
51655-029-25	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220909	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	6.25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-25)
51655-029-26	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20221122	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	6.25 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-029-26)
51655-029-52	51655-029	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20150209	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	6.25 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-029-52)
51655-030-25	51655-030	HUMAN PRESCRIPTION DRUG	Carvedilol	Carvedilol	TABLET, FILM COATED	ORAL	20220413	N/A	ANDA	ANDA077614	Northwind Health Company, LLC	CARVEDILOL	12.5 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-030-25)