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
68071-2587-9	68071-2587	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211202	N/A	ANDA	ANDA204598	NuCare Pharmaceuticals,Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68071-2587-9)
68788-8106-6	68788-8106	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211103	N/A	ANDA	ANDA204598	Preferred Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68788-8106-6)
68788-8106-3	68788-8106	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211103	N/A	ANDA	ANDA204598	Preferred Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (68788-8106-3)
68788-8106-1	68788-8106	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211103	N/A	ANDA	ANDA204598	Preferred Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (68788-8106-1)
68788-8106-9	68788-8106	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211103	N/A	ANDA	ANDA204598	Preferred Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (68788-8106-9)
67046-1361-3	67046-1361	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20241112	N/A	ANDA	ANDA204598	Coupler LLC	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (67046-1361-3)
42291-045-90	42291-045	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20240104	N/A	ANDA	ANDA204598	AvKARE	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (42291-045-90)
50090-3044-0	50090-3044	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20170608	N/A	ANDA	ANDA204598	A-S Medication Solutions	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-3044-0)
50090-3056-0	50090-3056	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20170614	N/A	ANDA	ANDA204598	A-S Medication Solutions	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-3056-0)
31722-595-30	31722-595	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-595-30)
31722-596-30	31722-596	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (31722-596-30)
31722-596-31	31722-596	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	70 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-31)
31722-596-32	31722-596	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-596-32)
31722-596-90	31722-596	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-596-90)
31722-595-31	31722-595	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	48 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-31)
31722-595-32	31722-595	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	48 mg/1	100 TABLET, FILM COATED in 1 BLISTER PACK (31722-595-32)
31722-595-90	31722-595	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160714	N/A	ANDA	ANDA204598	Camber Pharmaceuticals, Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (31722-595-90)