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
68071-4009-1	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (68071-4009-1)
68071-4009-2	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (68071-4009-2)
68071-4009-3	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68071-4009-3)
68071-4009-4	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (68071-4009-4)
68071-4009-5	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (68071-4009-5)
68071-4009-6	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68071-4009-6)
68071-4009-7	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (68071-4009-7)
68071-4009-9	68071-4009	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20170719	N/A	ANDA	ANDA090796	NuCare Pharmaceuticals,Inc.	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-4009-9)
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)
80425-0243-4	80425-0243	HUMAN PRESCRIPTION DRUG	Ibuprofen	Ibuprofen	TABLET, FILM COATED	ORAL	20230110	N/A	ANDA	ANDA090796	Advanced Rx Pharmacy of Tennessee, LLC	IBUPROFEN	800 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (80425-0243-4)
71335-1503-0	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	21 TABLET, FILM COATED in 1 BOTTLE (71335-1503-0)
71335-1503-1	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1503-1)
71335-1503-2	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	15 TABLET, FILM COATED in 1 BOTTLE (71335-1503-2)
71335-1503-3	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1503-3)
71335-1503-4	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	40 TABLET, FILM COATED in 1 BOTTLE (71335-1503-4)
71335-1503-5	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-1503-5)
71335-1503-6	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1503-6)
71335-1503-7	71335-1503	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200212	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	600 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-1503-7)
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)
71335-1517-1	71335-1517	HUMAN PRESCRIPTION DRUG	IBUPROFEN	IBUPROFEN	TABLET, FILM COATED	ORAL	20200220	N/A	ANDA	ANDA090796	Bryant Ranch Prepack	IBUPROFEN	400 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1517-1)