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
51407-205-90	51407-205	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210323	N/A	ANDA	ANDA200884	Golden State Medical Supply, Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-205-90)
51407-204-90	51407-204	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210323	N/A	ANDA	ANDA200884	Golden State Medical Supply, Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (51407-204-90)
71335-0872-2	71335-0872	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180620	N/A	ANDA	ANDA200884	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-0872-2)
71335-0872-1	71335-0872	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20190307	N/A	ANDA	ANDA200884	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0872-1)
71335-0872-3	71335-0872	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20211227	N/A	ANDA	ANDA200884	Bryant Ranch Prepack	FENOFIBRATE	145 mg/1	28 TABLET, FILM COATED in 1 BOTTLE (71335-0872-3)
63304-448-30	63304-448	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-448-30)
63304-449-30	63304-449	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63304-449-30)
63304-449-90	63304-449	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63304-449-90)
63304-448-90	63304-448	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	48 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63304-448-90)
63304-449-05	63304-449	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	145 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63304-449-05)
63304-448-05	63304-448	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20180601	N/A	ANDA	ANDA200884	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	48 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (63304-448-05)
51655-433-52	51655-433	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20200917	N/A	ANDA	ANDA200884	Northwind Pharmaceuticals, LLC	FENOFIBRATE	145 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-433-52)
51655-554-52	51655-554	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20210121	N/A	ANDA	ANDA200884	Northwind Pharmaceuticals, LLC	FENOFIBRATE	48 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-554-52)
50090-5796-0	50090-5796	HUMAN PRESCRIPTION DRUG	Fenofibrate	fenofibrate	TABLET, FILM COATED	ORAL	20211013	N/A	ANDA	ANDA200884	A-S Medication Solutions	FENOFIBRATE	145 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-5796-0)