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
0115-1554-10	0115-1554	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20160912	N/A	NDA AUTHORIZED GENERIC	NDA022224	Amneal Pharmaceuticals of New York LLC	FENOFIBRIC ACID	45 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1554-10)
0115-1555-10	0115-1555	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20160912	N/A	NDA AUTHORIZED GENERIC	NDA022224	Amneal Pharmaceuticals of New York LLC	FENOFIBRIC ACID	135 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0115-1555-10)
0074-3162-90	0074-3162	HUMAN PRESCRIPTION DRUG	Trilipix	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20160912	N/A	NDA	NDA022224	AbbVie Inc.	FENOFIBRIC ACID	135 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-3162-90)
0074-3161-90	0074-3161	HUMAN PRESCRIPTION DRUG	Trilipix	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20160912	N/A	NDA	NDA022224	AbbVie Inc.	FENOFIBRIC ACID	45 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (0074-3161-90)