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
70518-1051-2	70518-1051	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201211	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-2)
70518-1051-4	70518-1051	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250721	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1051-4)
70518-1364-2	70518-1364	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201023	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1364-2)
70518-1364-4	70518-1364	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230730	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	27 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-4)
70518-1364-5	70518-1364	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230802	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1364-5)
70518-1364-7	70518-1364	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20250429	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1364-7)
70518-1409-0	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180911	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-0)
70518-1409-1	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180914	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-1)
70518-1409-2	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180917	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-2)
70518-1409-4	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180924	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-4)
70518-1409-5	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20181008	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	10 TABLET, FILM COATED in 1 BLISTER PACK (70518-1409-5)
70518-1409-9	70518-1409	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210520	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1409-9)
71335-0690-1	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20190201	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-0690-1)
71335-0690-2	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180219	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0690-2)
71335-0690-3	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180227	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-0690-3)
71335-0690-4	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180226	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0690-4)
71335-0690-5	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180726	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0690-5)
71335-0690-6	71335-0690	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180405	N/A	ANDA	ANDA091625	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0690-6)
72789-363-01	72789-363	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20231127	N/A	ANDA	ANDA091625	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-01)
72789-363-10	72789-363	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20231110	N/A	ANDA	ANDA091625	PD-Rx Pharmaceuticals, Inc.	IBUPROFEN	600 mg/1	10 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-363-10)