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
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)
50090-6167-0	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (50090-6167-0)
50090-6167-2	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE (50090-6167-2)
50090-6167-3	50090-6167	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20221013	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (50090-6167-3)
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)
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)
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)
76420-210-20	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (76420-210-20)
76420-210-30	76420-210	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20220308	N/A	ANDA	ANDA078420	Asclemed USA, Inc.	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (76420-210-30)
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)
71335-1391-1	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191209	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (71335-1391-1)
71335-1391-2	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191220	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (71335-1391-2)
71335-1391-3	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191114	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (71335-1391-3)
71335-1391-4	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20191107	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (71335-1391-4)
71335-1391-5	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20211228	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	42 TABLET in 1 BOTTLE (71335-1391-5)
71335-1391-6	71335-1391	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200713	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	56 TABLET in 1 BOTTLE (71335-1391-6)