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
33342-347-10	33342-347	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	90 TABLET in 1 CONTAINER (33342-347-10)
33342-347-12	33342-347	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	10 BLISTER PACK in 1 CARTON (33342-347-12) / 10 TABLET in 1 BLISTER PACK
33342-347-47	33342-347	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	54 mg/1	9 BLISTER PACK in 1 CARTON (33342-347-47) / 14 TABLET in 1 BLISTER PACK
33342-348-10	33342-348	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	90 TABLET in 1 CONTAINER (33342-348-10)
33342-348-12	33342-348	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	10 BLISTER PACK in 1 CARTON (33342-348-12) / 10 TABLET in 1 BLISTER PACK
33342-348-15	33342-348	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20260121	N/A	ANDA	ANDA210379	Macleods Pharmaceuticals Limited	FENOFIBRATE	160 mg/1	500 TABLET in 1 CONTAINER (33342-348-15)