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
68788-7765-8	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)
68788-7765-2	68788-7765	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200715	N/A	ANDA	ANDA078420	Preferred Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	20 TABLET in 1 BOTTLE (68788-7765-2)
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)
45865-111-60	45865-111	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200701	N/A	ANDA	ANDA078420	Medsource Pharmaceuticals	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (45865-111-60)
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)
50228-465-01	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)
72189-072-14	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	14 TABLET in 1 BOTTLE (72189-072-14)
72189-072-30	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (72189-072-30)
72189-072-60	72189-072	HUMAN PRESCRIPTION DRUG	NABUMETONE	NABUMETONE	TABLET	ORAL	20200618	N/A	ANDA	ANDA078420	direct rx	NABUMETONE	750 mg/1	60 TABLET in 1 BOTTLE (72189-072-60)
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)
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)
50228-466-30	50228-466	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190626	N/A	ANDA	ANDA078420	ScieGen Pharmaceuticals Inc	NABUMETONE	750 mg/1	30 TABLET in 1 BOTTLE (50228-466-30)
69367-242-01	69367-242	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	750 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (69367-242-01)
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)