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
71205-978-90	71205-978	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	750 mg/1	90 TABLET in 1 BOTTLE, PLASTIC (71205-978-90)
71205-977-30	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (71205-977-30)
71205-977-55	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (71205-977-55)
71205-977-60	71205-977	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20200507	N/A	ANDA	ANDA078420	Proficient Rx LP	NABUMETONE	500 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (71205-977-60)
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)
50228-466-05	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)
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)
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)
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)
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)
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)
69367-241-01	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (69367-241-01)
69367-241-05	69367-241	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	500 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (69367-241-05)
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)
69367-242-05	69367-242	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET	ORAL	20190925	N/A	ANDA	ANDA078420	Westminster Pharmaceuticals, LLC	NABUMETONE	750 mg/1	500 TABLET in 1 BOTTLE, PLASTIC (69367-242-05)