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
42385-951-11	42385-951	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	145 mg/1	1000 TABLET in 1 BOTTLE (42385-951-11)
42385-951-30	42385-951	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	145 mg/1	30 TABLET in 1 BOTTLE (42385-951-30)
42385-951-90	42385-951	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (42385-951-90)
42385-950-90	42385-950	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	48 mg/1	90 TABLET in 1 BOTTLE (42385-950-90)
42385-950-30	42385-950	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	48 mg/1	30 TABLET in 1 BOTTLE (42385-950-30)
42385-950-11	42385-950	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Laurus Labs Limited	FENOFIBRATE	48 mg/1	1000 TABLET in 1 BOTTLE (42385-950-11)
68071-1712-9	68071-1712	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20230301	N/A	ANDA	ANDA211122	NuCare Pharmaceuticals,Inc.	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (68071-1712-9)
69844-012-01	69844-012	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	48 mg/1	30 TABLET in 1 BOTTLE (69844-012-01)
69844-012-02	69844-012	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	48 mg/1	90 TABLET in 1 BOTTLE (69844-012-02)
69844-012-03	69844-012	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	48 mg/1	1000 TABLET in 1 BOTTLE (69844-012-03)
69844-013-01	69844-013	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	145 mg/1	30 TABLET in 1 BOTTLE (69844-013-01)
69844-013-02	69844-013	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (69844-013-02)
69844-013-03	69844-013	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20200318	N/A	ANDA	ANDA211122	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	145 mg/1	1000 TABLET in 1 BOTTLE (69844-013-03)
69315-287-09	69315-287	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20220718	N/A	ANDA	ANDA211122	Leading Pharma, LLC	FENOFIBRATE	48 mg/1	90 TABLET in 1 BOTTLE (69315-287-09)
69315-288-05	69315-288	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20220718	N/A	ANDA	ANDA211122	Leading Pharma, LLC	FENOFIBRATE	145 mg/1	500 TABLET in 1 BOTTLE (69315-288-05)
69315-288-09	69315-288	HUMAN PRESCRIPTION DRUG	fenofibrate	fenofibrate	TABLET	ORAL	20220718	N/A	ANDA	ANDA211122	Leading Pharma, LLC	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (69315-288-09)