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
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)
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)
68788-7597-9	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE (68788-7597-9)
50228-465-01	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (50228-465-01)
50228-465-05	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (50228-465-05)
50228-465-30	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (50228-465-30)
72189-072-60	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (72189-072-60)
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)
71205-978-60	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-978-60)
71205-978-72	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	120 TABLET in 1 BOTTLE, PLASTIC (71205-978-72)
71205-978-90	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-978-90)
80425-0054-1	80425-0054	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx of Tennessee, LLC	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (80425-0054-1)
80425-0054-2	80425-0054	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx of Tennessee, LLC	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (80425-0054-2)
76420-210-10	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	10 TABLET in 1 BOTTLE (76420-210-10)
76420-210-14	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE (76420-210-14)