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
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)
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)
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)