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
43598-909-90	43598-909	HUMAN PRESCRIPTION DRUG	Fenofibrate	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200131	N/A	ANDA	ANDA210670	Dr. Reddy's Laboratories Inc.	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-909-90)
43598-910-05	43598-910	HUMAN PRESCRIPTION DRUG	Fenofibrate	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200131	N/A	ANDA	ANDA210670	Dr. Reddy's Laboratories Inc.	FENOFIBRATE	160 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (43598-910-05)
43598-910-90	43598-910	HUMAN PRESCRIPTION DRUG	Fenofibrate	FENOFIBRATE	TABLET, FILM COATED	ORAL	20200131	N/A	ANDA	ANDA210670	Dr. Reddy's Laboratories Inc.	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (43598-910-90)
72162-2170-9	72162-2170	HUMAN PRESCRIPTION DRUG	Fenofibrate	FENOFIBRATE	TABLET, FILM COATED	ORAL	20231207	N/A	ANDA	ANDA210670	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (72162-2170-9)