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
71335-1756-1	71335-1756	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20211220	N/A	ANDA	ANDA213864	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE (71335-1756-1)
71335-1756-2	71335-1756	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20211220	N/A	ANDA	ANDA213864	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (71335-1756-2)
71335-1756-3	71335-1756	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20211220	N/A	ANDA	ANDA213864	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	60 TABLET in 1 BOTTLE (71335-1756-3)
71335-1756-4	71335-1756	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20211220	N/A	ANDA	ANDA213864	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	28 TABLET in 1 BOTTLE (71335-1756-4)
71335-1756-5	71335-1756	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20211220	N/A	ANDA	ANDA213864	Bryant Ranch Prepack	FENOFIBRATE	160 mg/1	100 TABLET in 1 BOTTLE (71335-1756-5)
70518-2947-0	70518-2947	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20201127	N/A	ANDA	ANDA213864	REMEDYREPACK INC.	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-2947-0)
68788-7816-9	68788-7816	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20201106	N/A	ANDA	ANDA213864	Preferred Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	60 TABLET in 1 BOTTLE (68788-7816-9)
68788-7816-3	68788-7816	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20201106	N/A	ANDA	ANDA213864	Preferred Pharmaceuticals Inc.	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE (68788-7816-3)
0904-7539-04	0904-7539	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20250522	N/A	ANDA	ANDA213864	Major Pharmaceuticals	FENOFIBRATE	160 mg/1	30 BLISTER PACK in 1 CARTON (0904-7539-04) / 1 TABLET in 1 BLISTER PACK
70756-214-51	70756-214	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20200910	N/A	ANDA	ANDA213864	Lifestar Pharma LLC	FENOFIBRATE	54 mg/1	500 TABLET in 1 BOTTLE (70756-214-51)
70756-214-90	70756-214	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20200910	N/A	ANDA	ANDA213864	Lifestar Pharma LLC	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE (70756-214-90)
60760-318-30	60760-318	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20210114	N/A	ANDA	ANDA213864	St. Mary's Medical Park Pharmacy	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (60760-318-30)
72603-840-01	72603-840	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20250929	N/A	ANDA	ANDA213864	NorthStar RxLLC	FENOFIBRATE	54 mg/1	90 TABLET in 1 BOTTLE (72603-840-01)
70756-215-51	70756-215	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20200910	N/A	ANDA	ANDA213864	Lifestar Pharma LLC	FENOFIBRATE	160 mg/1	500 TABLET in 1 BOTTLE (70756-215-51)
70756-215-90	70756-215	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20200910	N/A	ANDA	ANDA213864	Lifestar Pharma LLC	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (70756-215-90)
51655-856-52	51655-856	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20230213	N/A	ANDA	ANDA213864	Northwind Pharmaceuticals, LLC	FENOFIBRATE	160 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (51655-856-52)
72603-841-01	72603-841	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20250929	N/A	ANDA	ANDA213864	NorthStar RxLLC	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE (72603-841-01)
72603-841-02	72603-841	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20250929	N/A	ANDA	ANDA213864	NorthStar RxLLC	FENOFIBRATE	160 mg/1	500 TABLET in 1 BOTTLE (72603-841-02)
70518-2907-1	70518-2907	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20210113	N/A	ANDA	ANDA213864	REMEDYREPACK INC.	FENOFIBRATE	160 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (70518-2907-1)
71205-666-30	71205-666	HUMAN PRESCRIPTION DRUG	FENOFIBRATE	FENOFIBRATE	TABLET	ORAL	20220601	N/A	ANDA	ANDA213864	Proficient Rx LP	FENOFIBRATE	54 mg/1	30 TABLET in 1 BOTTLE (71205-666-30)