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
72189-184-30	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)
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)