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
68788-7765-3	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (68788-7765-3)
68788-7765-6	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (68788-7765-6)
68788-7765-8	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	120 TABLET in 1 BOTTLE (68788-7765-8)
68788-7765-9	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (68788-7765-9)
63629-8506-1	63629-8506	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (63629-8506-1)
63629-8508-1	63629-8508	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (63629-8508-1)
63629-8509-1	63629-8509	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (63629-8509-1)
63629-8510-1	63629-8510	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	Bryant Ranch Prepack	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (63629-8510-1)
50228-465-01	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE (50228-465-01)
50228-465-05	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE (50228-465-05)
50228-465-30	50228-465	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (50228-465-30)
50090-5294-0	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE (50090-5294-0)
50090-5294-7	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE (50090-5294-7)
50090-5294-8	50090-5294	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20201023	N/A	ANDA	ANDA078420	A-S Medication Solutions	NABUMETONE	500 mg/1	90 TABLET in 1 BOTTLE (50090-5294-8)
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)
50228-466-01	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE (50228-466-01)
50228-466-05	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE (50228-466-05)