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
71335-1391-7	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20211228	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE (71335-1391-7)
71335-1391-8	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20211228	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (71335-1391-8)
71335-1391-9	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20211228	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	9 TABLET in 1 BOTTLE (71335-1391-9)
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)
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)
76420-210-60	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (76420-210-60)
55700-845-60	55700-845	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200228	20270331	ANDA	ANDA078420	Quality Care Products, LLC	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (55700-845-60)
72189-184-14	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	14 TABLET in 1 BOTTLE (72189-184-14)
72189-184-30	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (72189-184-30)
72189-184-60	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (72189-184-60)
72189-184-90	72189-184	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20210511	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (72189-184-90)
69367-241-01	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (69367-241-01)
69367-241-05	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (69367-241-05)
71335-2293-1	71335-2293	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20231201	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (71335-2293-1)
76420-210-07	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	7 TABLET in 1 BOTTLE (76420-210-07)
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)