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
62207-356-43	62207-356	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20150921	N/A	ANDA	ANDA091625	Granules India Limited	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (62207-356-43)
62207-356-47	62207-356	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20150921	N/A	ANDA	ANDA091625	Granules India Limited	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (62207-356-47)
62207-356-49	62207-356	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20150921	N/A	ANDA	ANDA091625	Granules India Limited	IBUPROFEN	800 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (62207-356-49)
62207-356-54	62207-356	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20150921	N/A	ANDA	ANDA091625	Granules India Limited	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (62207-356-54)
67877-319-01	67877-319	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	400 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-319-01)
67877-319-05	67877-319	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	400 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-319-05)
67877-319-30	67877-319	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-319-30)
67877-319-50	67877-319	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	400 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (67877-319-50)
67877-320-01	67877-320	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-320-01)
67877-320-05	67877-320	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-320-05)
67877-320-30	67877-320	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-320-30)
67877-320-50	67877-320	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (67877-320-50)
67877-321-01	67877-321	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (67877-321-01)
67877-321-05	67877-321	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (67877-321-05)
67877-321-30	67877-321	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (67877-321-30)
67877-321-50	67877-321	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151221	N/A	ANDA	ANDA091625	Ascend Laboratories, LLC	IBUPROFEN	800 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (67877-321-50)
70518-0176-2	70518-0176	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180419	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0176-2)
70518-0761-0	70518-0761	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20171006	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-0)
70518-0761-1	70518-0761	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20171006	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-1)
70518-0761-2	70518-0761	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20180726	N/A	ANDA	ANDA091625	REMEDYREPACK INC.	IBUPROFEN	600 mg/1	28 TABLET, FILM COATED in 1 BLISTER PACK (70518-0761-2)