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
63187-378-30	63187-378	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20160901	N/A	ANDA	ANDA078671	Proficient Rx LP	NABUMETONE	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (63187-378-30)
63187-378-60	63187-378	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20160901	N/A	ANDA	ANDA078671	Proficient Rx LP	NABUMETONE	750 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (63187-378-60)
76282-258-05	76282-258	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20150414	N/A	ANDA	ANDA078671	Exelan Pharmaceuticals Inc.	NABUMETONE	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76282-258-05)
76282-257-01	76282-257	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20150414	N/A	ANDA	ANDA078671	Exelan Pharmaceuticals Inc.	NABUMETONE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76282-257-01)
76282-257-05	76282-257	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20150414	N/A	ANDA	ANDA078671	Exelan Pharmaceuticals Inc.	NABUMETONE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (76282-257-05)
76282-258-01	76282-258	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20150414	N/A	ANDA	ANDA078671	Exelan Pharmaceuticals Inc.	NABUMETONE	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (76282-258-01)