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
60687-655-21	60687-655	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20221202	20240731	ANDA	ANDA076635	American Health Packaging	FENOFIBRATE	54 mg/1	30 BLISTER PACK in 1 CARTON (60687-655-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-655-11)
50090-1275-0	50090-1275	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200918	N/A	ANDA	ANDA076635	A-S Medication Solutions	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (50090-1275-0)
50090-1275-1	50090-1275	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200918	N/A	ANDA	ANDA076635	A-S Medication Solutions	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (50090-1275-1)
63629-2505-1	63629-2505	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210309	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-2505-1)
43353-001-19	43353-001	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20150307	N/A	ANDA	ANDA076635	Aphena Pharma Solutions - Tennessee, LLC	FENOFIBRATE	160 mg/1	3060 TABLET, FILM COATED in 1 BOTTLE (43353-001-19)
63187-640-60	63187-640	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	54 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-640-60)
63187-640-30	63187-640	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	54 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-640-30)
63187-640-90	63187-640	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20160201	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-640-90)
63629-1099-1	63629-1099	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201118	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63629-1099-1)
63629-1099-2	63629-1099	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210525	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63629-1099-2)
63629-1099-3	63629-1099	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20201102	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-1099-3)
63629-1099-4	63629-1099	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20210517	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (63629-1099-4)
63629-1100-1	63629-1100	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211130	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	54 mg/1	50 TABLET, FILM COATED in 1 BOTTLE (63629-1100-1)
63629-1100-2	63629-1100	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20211130	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-1100-2)
63629-1101-1	63629-1101	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200918	N/A	ANDA	ANDA076635	Bryant Ranch Prepack	FENOFIBRATE	54 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63629-1101-1)
63187-760-60	63187-760	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20161101	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	160 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-760-60)
63187-760-90	63187-760	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20161101	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	160 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (63187-760-90)
63187-760-30	63187-760	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20161101	N/A	ANDA	ANDA076635	Proficient Rx LP	FENOFIBRATE	160 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-760-30)
63304-900-10	63304-900	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200918	N/A	ANDA	ANDA076635	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	54 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-900-10)
63304-901-10	63304-901	HUMAN PRESCRIPTION DRUG	Fenofibrate	Fenofibrate	TABLET, FILM COATED	ORAL	20200918	N/A	ANDA	ANDA076635	Sun Pharmaceutical Industries, Inc.	FENOFIBRATE	160 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (63304-901-10)