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
71335-1234-9	71335-1234	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220502	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	500 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (71335-1234-9)
71205-030-20	71205-030	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220119	N/A	ANDA	ANDA091083	Proficient Rx LP	NABUMETONE	500 mg/1	20 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-20)
71205-030-30	71205-030	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA091083	Proficient Rx LP	NABUMETONE	500 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-30)
71205-030-60	71205-030	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA091083	Proficient Rx LP	NABUMETONE	500 mg/1	60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-60)
71205-030-90	71205-030	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20180501	N/A	ANDA	ANDA091083	Proficient Rx LP	NABUMETONE	500 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (71205-030-90)
0591-3671-01	0591-3671	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20110613	N/A	ANDA	ANDA091083	Actavis Pharma, Inc.	NABUMETONE	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3671-01)
0591-3671-05	0591-3671	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20110613	N/A	ANDA	ANDA091083	Actavis Pharma, Inc.	NABUMETONE	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (0591-3671-05)
63187-307-30	63187-307	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190101	N/A	ANDA	ANDA091083	Proficient Rx LP	NABUMETONE	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (63187-307-30)