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
65862-768-90	65862-768	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	48 mg/1	90 TABLET, COATED in 1 BOTTLE (65862-768-90)
65862-768-99	65862-768	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	48 mg/1	1000 TABLET, COATED in 1 BOTTLE (65862-768-99)
65862-769-01	65862-769	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	145 mg/1	100 TABLET, COATED in 1 BOTTLE (65862-769-01)
65862-768-78	65862-768	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	48 mg/1	10 BLISTER PACK in 1 CARTON (65862-768-78) / 10 TABLET, COATED in 1 BLISTER PACK (65862-768-10)
65862-768-05	65862-768	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	48 mg/1	500 TABLET, COATED in 1 BOTTLE (65862-768-05)
65862-768-01	65862-768	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	48 mg/1	100 TABLET, COATED in 1 BOTTLE (65862-768-01)
65862-769-05	65862-769	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	145 mg/1	500 TABLET, COATED in 1 BOTTLE (65862-769-05)
65862-769-78	65862-769	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	145 mg/1	10 BLISTER PACK in 1 CARTON (65862-769-78) / 10 TABLET, COATED in 1 BLISTER PACK (65862-769-10)
65862-769-90	65862-769	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	145 mg/1	90 TABLET, COATED in 1 BOTTLE (65862-769-90)
65862-769-99	65862-769	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20160505	N/A	ANDA	ANDA205118	Aurobindo Pharma Limited	FENOFIBRATE	145 mg/1	1000 TABLET, COATED in 1 BOTTLE (65862-769-99)
82009-060-90	82009-060	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20221118	N/A	ANDA	ANDA205118	QUALLENT PHARMACEUTICALS HEALTH LLC	FENOFIBRATE	145 mg/1	90 TABLET, COATED in 1 BOTTLE (82009-060-90)
71335-1701-1	71335-1701	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20210112	N/A	ANDA	ANDA205118	Bryant Ranch Prepack	FENOFIBRATE	48 mg/1	30 TABLET, COATED in 1 BOTTLE (71335-1701-1)
71335-1701-2	71335-1701	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20200908	N/A	ANDA	ANDA205118	Bryant Ranch Prepack	FENOFIBRATE	48 mg/1	90 TABLET, COATED in 1 BOTTLE (71335-1701-2)
71335-1701-3	71335-1701	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20211229	N/A	ANDA	ANDA205118	Bryant Ranch Prepack	FENOFIBRATE	48 mg/1	28 TABLET, COATED in 1 BOTTLE (71335-1701-3)
50090-3887-0	50090-3887	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, COATED	ORAL	20181130	N/A	ANDA	ANDA205118	A-S Medication Solutions	FENOFIBRATE	48 mg/1	90 TABLET, COATED in 1 BOTTLE (50090-3887-0)