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
60687-618-21	60687-618	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20210809	N/A	ANDA	ANDA090856	American Health Packaging	FENOFIBRATE	48 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-618-21) / 1 TABLET in 1 BLISTER PACK (60687-618-11)
60687-629-01	60687-629	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20230308	N/A	ANDA	ANDA090856	American Health Packaging	FENOFIBRATE	145 mg/1	100 BLISTER PACK in 1 CARTON (60687-629-01) / 1 TABLET in 1 BLISTER PACK (60687-629-11)
60687-629-21	60687-629	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20210624	N/A	ANDA	ANDA090856	American Health Packaging	FENOFIBRATE	145 mg/1	30 BLISTER PACK in 1 BOX, UNIT-DOSE (60687-629-21) / 1 TABLET in 1 BLISTER PACK (60687-629-11)
68180-388-09	68180-388	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20200801	N/A	ANDA	ANDA090856	Lupin Pharmaceuticals, Inc.	FENOFIBRATE	48 mg/1	90 TABLET in 1 BOTTLE (68180-388-09)
68180-389-02	68180-389	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20200801	N/A	ANDA	ANDA090856	Lupin Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	500 TABLET in 1 BOTTLE (68180-389-02)
68180-389-09	68180-389	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20200801	N/A	ANDA	ANDA090856	Lupin Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (68180-389-09)
50268-338-12	50268-338	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20220922	N/A	ANDA	ANDA090856	AvPAK	FENOFIBRATE	48 mg/1	20 BLISTER PACK in 1 BOX (50268-338-12) / 1 TABLET in 1 BLISTER PACK (50268-338-11)
82868-018-30	82868-018	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20231017	N/A	ANDA	ANDA090856	Northwind Pharmaceuticals, LLC	FENOFIBRATE	145 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (82868-018-30)