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
43063-972-20	43063-972	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190422	N/A	ANDA	ANDA078671	PD-Rx Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-20)
43063-972-30	43063-972	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190710	N/A	ANDA	ANDA078671	PD-Rx Pharmaceuticals, Inc.	NABUMETONE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-972-30)
69097-965-07	69097-965	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA078671	Cipla USA Inc.	NABUMETONE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69097-965-07)
69097-965-12	69097-965	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA078671	Cipla USA Inc.	NABUMETONE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69097-965-12)
51655-396-25	51655-396	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20200707	N/A	ANDA	ANDA078671	Northwind Pharmaceuticals, LLC	NABUMETONE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-396-25)
69097-966-07	69097-966	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA078671	Cipla USA Inc.	NABUMETONE	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (69097-966-07)
69097-966-12	69097-966	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA078671	Cipla USA Inc.	NABUMETONE	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (69097-966-12)
80425-0053-1	80425-0053	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190306	N/A	ANDA	ANDA078671	Advanced Rx of Tennessee, LLC	NABUMETONE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0053-1)
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)
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)
60687-630-21	60687-630	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220323	N/A	ANDA	ANDA078671	American Health Packaging	NABUMETONE	500 mg/1	30 BLISTER PACK in 1 CARTON (60687-630-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-630-11)
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)