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
71335-1272-2	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (71335-1272-2)
71335-1272-3	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20190717	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-1272-3)
71335-1272-4	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	20 TABLET, FILM COATED in 1 BOTTLE (71335-1272-4)
71335-1272-5	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	42 TABLET, FILM COATED in 1 BOTTLE (71335-1272-5)
71335-1272-6	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (71335-1272-6)
71335-1272-7	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-1272-7)
71335-1272-8	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	6 TABLET, FILM COATED in 1 BOTTLE (71335-1272-8)
71335-1272-9	71335-1272	HUMAN PRESCRIPTION DRUG	Nabumetone	Nabumetone	TABLET, FILM COATED	ORAL	20220629	N/A	ANDA	ANDA091083	Bryant Ranch Prepack	NABUMETONE	750 mg/1	9 TABLET, FILM COATED in 1 BOTTLE (71335-1272-9)