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
71335-2628-1	71335-2628	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250414	N/A	ANDA	ANDA217732	Bryant Ranch Prepack	FENOFIBRATE	40 mg/1	90 TABLET in 1 BOTTLE (71335-2628-1)
72162-2469-9	72162-2469	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250414	N/A	ANDA	ANDA217732	Bryant Ranch Prepack	FENOFIBRATE	40 mg/1	90 TABLET in 1 BOTTLE (72162-2469-9)
71335-2629-1	71335-2629	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250414	N/A	ANDA	ANDA217732	Bryant Ranch Prepack	FENOFIBRATE	120 mg/1	90 TABLET in 1 BOTTLE (71335-2629-1)
72162-2470-9	72162-2470	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250414	N/A	ANDA	ANDA217732	Bryant Ranch Prepack	FENOFIBRATE	120 mg/1	90 TABLET in 1 BOTTLE (72162-2470-9)
73352-101-01	73352-101	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250812	N/A	ANDA	ANDA217732	Trifluent Pharma LLC	FENOFIBRATE	40 mg/1	90 TABLET in 1 BOTTLE (73352-101-01)
82619-101-01	82619-101	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20230920	N/A	ANDA	ANDA217732	Creekwood Pharmaceuticals LLC	FENOFIBRATE	40 mg/1	90 TABLET in 1 BOTTLE (82619-101-01)
73352-102-01	73352-102	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20250812	N/A	ANDA	ANDA217732	Trifluent Pharma LLC	FENOFIBRATE	120 mg/1	90 TABLET in 1 BOTTLE (73352-102-01)
82619-102-01	82619-102	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	fenofibrate	TABLET	ORAL	20230920	N/A	ANDA	ANDA217732	Creekwood Pharmaceuticals LLC	FENOFIBRATE	120 mg/1	90 TABLET in 1 BOTTLE (82619-102-01)