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
71335-1559-9	71335-1559	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220210	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	9 TABLET in 1 BOTTLE (71335-1559-9)
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)
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)
72789-040-30	72789-040	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191217	N/A	ANDA	ANDA078420	PD-Rx Pharmaceuticals, Inc.	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (72789-040-30)
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)
80425-0104-1	80425-0104	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Advanced Rx Pharmacy of Tennessee, LLC	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (80425-0104-1)
80425-0104-2	80425-0104	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20230407	N/A	ANDA	ANDA078420	Advanced Rx Pharmacy of Tennessee, LLC	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (80425-0104-2)
80425-0104-3	80425-0104	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20230407	N/A	ANDA	ANDA078420	Advanced Rx Pharmacy of Tennessee, LLC	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE (80425-0104-3)
68788-7597-1	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (68788-7597-1)
68788-7597-2	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	20 TABLET in 1 BOTTLE (68788-7597-2)
68788-7597-3	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (68788-7597-3)
68788-7597-6	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (68788-7597-6)
68788-7597-8	68788-7597	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200213	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals Inc.	NABUMETONE	750 mg/1	120 TABLET in 1 BOTTLE (68788-7597-8)
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)