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
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)
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)
71335-2292-1	71335-2292	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20231201	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (71335-2292-1)
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)
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)
68788-7765-1	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (68788-7765-1)