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
43975-305-10	43975-305	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20180501	N/A	ANDA	ANDA209504	ANI Pharmaceuticals, Inc.	FENOFIBRATE	134 mg/1	100 CAPSULE in 1 BOTTLE (43975-305-10)
43975-305-50	43975-305	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20180501	N/A	ANDA	ANDA209504	ANI Pharmaceuticals, Inc.	FENOFIBRATE	134 mg/1	500 CAPSULE in 1 BOTTLE (43975-305-50)
43975-306-10	43975-306	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20180501	N/A	ANDA	ANDA209504	ANI Pharmaceuticals, Inc.	FENOFIBRATE	200 mg/1	100 CAPSULE in 1 BOTTLE (43975-306-10)
43975-306-50	43975-306	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20180501	N/A	ANDA	ANDA209504	ANI Pharmaceuticals, Inc.	FENOFIBRATE	200 mg/1	500 CAPSULE in 1 BOTTLE (43975-306-50)
43975-444-10	43975-444	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20180501	N/A	ANDA	ANDA209504	ANI Pharmaceuticals, Inc.	FENOFIBRATE	67 mg/1	100 CAPSULE in 1 BOTTLE (43975-444-10)
68071-2812-3	68071-2812	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20220815	N/A	ANDA	ANDA209504	NuCare Pharmaceuticals,Inc.	FENOFIBRATE	134 mg/1	30 CAPSULE in 1 BOTTLE (68071-2812-3)