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
69315-289-09	69315-289	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20220820	N/A	ANDA	ANDA210606	Leading Pharma, LLC	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69315-289-09)
69315-290-05	69315-290	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20220820	N/A	ANDA	ANDA210606	Leading Pharma, LLC	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69315-290-05)
69315-290-09	69315-290	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20220820	N/A	ANDA	ANDA210606	Leading Pharma, LLC	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (69315-290-09)
42385-935-05	42385-935	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	54 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42385-935-05)
42385-935-11	42385-935	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	54 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42385-935-11)
42385-935-30	42385-935	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	54 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42385-935-30)
42385-935-90	42385-935	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42385-935-90)
42385-936-05	42385-936	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (42385-936-05)
42385-936-11	42385-936	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	160 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (42385-936-11)
42385-936-30	42385-936	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (42385-936-30)
42385-936-90	42385-936	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200113	N/A	ANDA	ANDA210606	Laurus Labs Limited	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42385-936-90)
69844-008-01	69844-008	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	54 mg/1	30 TABLET in 1 BOTTLE (69844-008-01)
69844-008-02	69844-008	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE (69844-008-02)
69844-008-03	69844-008	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	54 mg/1	1000 TABLET in 1 BOTTLE (69844-008-03)
69844-009-01	69844-009	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE (69844-009-01)
69844-009-02	69844-009	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (69844-009-02)
69844-009-03	69844-009	HUMAN PRESCRIPTION DRUG	Fenofibrate film coated	fenofibrate	TABLET	ORAL	20180817	N/A	ANDA	ANDA210606	Graviti Pharmaceuticals Private Limited	FENOFIBRATE	160 mg/1	1000 TABLET in 1 BOTTLE (69844-009-03)