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
80425-0054-2	80425-0054	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx Pharmacy of Tennessee, LLC	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (80425-0054-2)
53002-6960-2	53002-6960	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210501	N/A	ANDA	ANDA078420	RPK Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (53002-6960-2)
53002-6960-3	53002-6960	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210501	N/A	ANDA	ANDA078420	RPK Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (53002-6960-3)
72162-1558-1	72162-1558	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (72162-1558-1)
72162-1558-5	72162-1558	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (72162-1558-5)
63629-8510-1	63629-8510	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (63629-8510-1)
68788-7765-3	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (68788-7765-3)
68788-7765-6	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (68788-7765-6)
68788-7765-8	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	120 TABLET in 1 BOTTLE (68788-7765-8)
68788-7765-9	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (68788-7765-9)
71205-530-30	71205-530	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210203	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (71205-530-30)
71205-530-60	71205-530	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210203	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (71205-530-60)
71205-530-90	71205-530	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20210203	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE (71205-530-90)
72162-1557-1	72162-1557	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (72162-1557-1)
72162-1557-5	72162-1557	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20240208	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (72162-1557-5)
63629-8509-1	63629-8509	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (63629-8509-1)
50090-6167-4	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	20 TABLET in 1 BOTTLE (50090-6167-4)
71205-978-00	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (71205-978-00)
71205-978-30	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-978-30)
71205-978-55	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71205-978-55)