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
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)
68071-5135-0	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)
70518-2432-1	70518-2432	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210526	N/A	ANDA	ANDA090796	REMEDYREPACK INC.	IBUPROFEN	400 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (70518-2432-1)
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)
51655-275-20	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20210709	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-20)
51655-275-21	51655-275	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20201029	N/A	ANDA	ANDA090796	Northwind Health Company, LLC	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-275-21)
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)
71335-1396-0	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-1396-0)
71335-1396-1	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1396-1)
71335-1396-2	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1396-2)
71335-1396-3	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1396-3)
71335-1396-4	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1396-4)
71335-1396-5	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1396-5)
71335-1396-6	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1396-6)
71335-1396-7	71335-1396	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20191118	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1396-7)
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)