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
33342-340-07	33342-340	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	30 TABLET in 1 BOTTLE (33342-340-07)
33342-340-10	33342-340	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	90 TABLET in 1 BOTTLE (33342-340-10)
33342-340-12	33342-340	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	10 BLISTER PACK in 1 CARTON (33342-340-12) / 10 TABLET in 1 BLISTER PACK
33342-340-15	33342-340	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	145 mg/1	500 TABLET in 1 BOTTLE (33342-340-15)
33342-339-07	33342-339	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	30 TABLET in 1 BOTTLE (33342-339-07)
33342-339-10	33342-339	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	90 TABLET in 1 BOTTLE (33342-339-10)
33342-339-12	33342-339	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	10 BLISTER PACK in 1 CARTON (33342-339-12) / 10 TABLET in 1 BLISTER PACK
33342-339-15	33342-339	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET	ORAL	20241113	N/A	ANDA	ANDA210248	Macleods Pharmaceuticals Limited	FENOFIBRATE	48 mg/1	500 TABLET in 1 BOTTLE (33342-339-15)