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
68180-232-09	68180-232	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20200701	N/A	ANDA	ANDA204019	Lupin Pharmaceuticals, Inc.	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (68180-232-09)
68180-231-09	68180-231	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20200701	N/A	ANDA	ANDA204019	Lupin Pharmaceuticals, Inc.	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE (68180-231-09)
50090-5854-1	50090-5854	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20211111	N/A	ANDA	ANDA204019	A-S Medication Solutions	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (50090-5854-1)
50090-5854-0	50090-5854	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20211111	N/A	ANDA	ANDA204019	A-S Medication Solutions	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE (50090-5854-0)
50090-6227-0	50090-6227	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20221114	N/A	ANDA	ANDA204019	A-S Medication Solutions	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE (50090-6227-0)
50090-6227-1	50090-6227	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20221114	N/A	ANDA	ANDA204019	A-S Medication Solutions	FENOFIBRATE	54 mg/1	30 TABLET in 1 BOTTLE (50090-6227-1)