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
42571-347-30	42571-347	HUMAN PRESCRIPTION DRUG	Fenofibric acid	Fenofibric acid	CAPSULE, DELAYED RELEASE	ORAL	20200901	N/A	ANDA	ANDA213450	Micro Labs Limited	FENOFIBRIC ACID	45 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42571-347-30)
42571-347-90	42571-347	HUMAN PRESCRIPTION DRUG	Fenofibric acid	Fenofibric acid	CAPSULE, DELAYED RELEASE	ORAL	20200901	N/A	ANDA	ANDA213450	Micro Labs Limited	FENOFIBRIC ACID	45 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42571-347-90)
42571-348-05	42571-348	HUMAN PRESCRIPTION DRUG	Fenofibric acid	Fenofibric acid	CAPSULE, DELAYED RELEASE	ORAL	20200901	N/A	ANDA	ANDA213450	Micro Labs Limited	FENOFIBRIC ACID	135 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42571-348-05)
42571-348-30	42571-348	HUMAN PRESCRIPTION DRUG	Fenofibric acid	Fenofibric acid	CAPSULE, DELAYED RELEASE	ORAL	20200901	N/A	ANDA	ANDA213450	Micro Labs Limited	FENOFIBRIC ACID	135 mg/1	30 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42571-348-30)
42571-348-90	42571-348	HUMAN PRESCRIPTION DRUG	Fenofibric acid	Fenofibric acid	CAPSULE, DELAYED RELEASE	ORAL	20200901	N/A	ANDA	ANDA213450	Micro Labs Limited	FENOFIBRIC ACID	135 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (42571-348-90)