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
49483-603-50	49483-603	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	600 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (49483-603-50)
49483-604-01	49483-604	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (49483-604-01)
49483-604-03	49483-604	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (49483-604-03)
49483-604-05	49483-604	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	800 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (49483-604-05)
49483-604-50	49483-604	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20151230	N/A	ANDA	ANDA090796	TIME CAP LABORATORIES, INC	IBUPROFEN	800 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (49483-604-50)
68071-4243-1	68071-4243	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180122	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-4243-1)
68071-4459-6	68071-4459	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20180531	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-4459-6)
68071-5126-3	68071-5126	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191211	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-5126-3)
68071-5126-9	68071-5126	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191211	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-5126-9)
68071-5134-6	68071-5134	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191213	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	400 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-5134-6)
68071-5135-0	68071-5135	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191216	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68071-5135-0)
68071-5140-3	68071-5140	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191231	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	3 TABLET, FILM COATED in 1 BOTTLE (68071-5140-3)
68071-5140-6	68071-5140	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200106	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	800 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (68071-5140-6)
70518-0005-6	70518-0005	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20230317	N/A	ANDA	ANDA090796	REMEDYREPACK INC.	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0005-6)
72189-231-21	72189-231	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210604	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (72189-231-21)
72189-231-30	72189-231	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210604	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-231-30)
72189-231-60	72189-231	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210604	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (72189-231-60)
72189-231-90	72189-231	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210604	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72189-231-90)
72189-266-30	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (72189-266-30)
72189-266-40	72189-266	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20210916	N/A	ANDA	ANDA090796	DIRECT RX	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (72189-266-40)