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
70436-169-06	70436-169	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20220411	N/A	ANDA	ANDA212562	Slate Run Pharmaceuticals, LLC	FENOFIBRIC ACID	135 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-169-06)
70436-169-03	70436-169	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20220411	N/A	ANDA	ANDA212562	Slate Run Pharmaceuticals, LLC	FENOFIBRIC ACID	135 mg/1	500 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-169-03)
70436-168-06	70436-168	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20220411	N/A	ANDA	ANDA212562	Slate Run Pharmaceuticals, LLC	FENOFIBRIC ACID	45 mg/1	90 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-168-06)
70436-168-03	70436-168	HUMAN PRESCRIPTION DRUG	Fenofibric Acid	Fenofibric Acid	CAPSULE, DELAYED RELEASE	ORAL	20220411	N/A	ANDA	ANDA212562	Slate Run Pharmaceuticals, LLC	FENOFIBRIC ACID	45 mg/1	1000 CAPSULE, DELAYED RELEASE in 1 BOTTLE (70436-168-03)