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
51079-599-20	51079-599	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20130610	N/A	ANDA	ANDA202856	Mylan Institutional Inc.	FENOFIBRATE	48 mg/1	100 BLISTER PACK in 1 CARTON (51079-599-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-599-01)
0378-3065-77	0378-3065	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20130514	N/A	ANDA	ANDA202856	Mylan Pharmaceuticals Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3065-77)
51079-608-20	51079-608	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20130610	N/A	ANDA	ANDA202856	Mylan Institutional Inc.	FENOFIBRATE	145 mg/1	100 BLISTER PACK in 1 CARTON (51079-608-20) / 1 TABLET, FILM COATED in 1 BLISTER PACK (51079-608-01)
68071-2686-9	68071-2686	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20220504	N/A	ANDA	ANDA202856	NuCare Pharmaceuticals,Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68071-2686-9)
68788-7932-1	68788-7932	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210615	N/A	ANDA	ANDA202856	Preferred Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PUMP (68788-7932-1)
68788-7932-3	68788-7932	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210615	N/A	ANDA	ANDA202856	Preferred Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-3)
68788-7932-6	68788-7932	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210615	N/A	ANDA	ANDA202856	Preferred Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-6)
68788-7932-9	68788-7932	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210615	N/A	ANDA	ANDA202856	Preferred Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (68788-7932-9)
50090-6934-0	50090-6934	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20231214	N/A	ANDA	ANDA202856	A-S Medication Solutions	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-6934-0)
0378-3066-05	0378-3066	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20130514	N/A	ANDA	ANDA202856	Mylan Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3066-05)
0378-3066-77	0378-3066	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20130514	N/A	ANDA	ANDA202856	Mylan Pharmaceuticals Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0378-3066-77)
50090-7242-0	50090-7242	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20240911	N/A	ANDA	ANDA202856	A-S Medication Solutions	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (50090-7242-0)
71335-2016-1	71335-2016	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA202856	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-2016-1)
71335-2016-2	71335-2016	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA202856	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-2016-2)
71335-2016-3	71335-2016	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20220210	N/A	ANDA	ANDA202856	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-2016-3)