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
72789-310-30	72789-310	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20220315	N/A	ANDA	ANDA201748	PD-Rx Pharmaceuticals, Inc.	FENOFIBRATE	130 mg/1	30 CAPSULE in 1 BOTTLE, PLASTIC (72789-310-30)
63304-443-05	63304-443	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20150302	N/A	ANDA	ANDA201748	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	43 mg/1	500 CAPSULE in 1 BOTTLE (63304-443-05)
63304-443-30	63304-443	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20150302	N/A	ANDA	ANDA201748	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	43 mg/1	30 CAPSULE in 1 BOTTLE (63304-443-30)
63304-444-05	63304-444	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20150302	N/A	ANDA	ANDA201748	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	130 mg/1	500 CAPSULE in 1 BOTTLE (63304-444-05)
63304-444-30	63304-444	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20150302	N/A	ANDA	ANDA201748	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	130 mg/1	30 CAPSULE in 1 BOTTLE (63304-444-30)
63304-444-90	63304-444	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	CAPSULE	ORAL	20150302	N/A	ANDA	ANDA201748	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	130 mg/1	90 CAPSULE in 1 BOTTLE (63304-444-90)