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
79739-7077-5	79739-7077	HUMAN PRESCRIPTION DRUG	Nabumetone 750 mg	Nabumetone	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	750 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (79739-7077-5)
79739-7078-1	79739-7078	HUMAN PRESCRIPTION DRUG	Nabumetone 1000 mg	Nabumetone	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	1000 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (79739-7078-1)
79739-7078-3	79739-7078	HUMAN PRESCRIPTION DRUG	Nabumetone 1000 mg	Nabumetone	TABLET, FILM COATED	ORAL	20191002	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	1000 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (79739-7078-3)
79739-7078-6	79739-7078	HUMAN PRESCRIPTION DRUG	Nabumetone 1000 mg	Nabumetone	TABLET, FILM COATED	ORAL	20200724	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	1000 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (79739-7078-6)
79739-7077-1	79739-7077	HUMAN PRESCRIPTION DRUG	Nabumetone 750 mg	Nabumetone	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	750 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (79739-7077-1)
79739-7076-5	79739-7076	HUMAN PRESCRIPTION DRUG	Nabumetone 500 mg	Nabumetone	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	500 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (79739-7076-5)
79739-7076-1	79739-7076	HUMAN PRESCRIPTION DRUG	Nabumetone 500 mg	Nabumetone	TABLET, FILM COATED	ORAL	20190904	N/A	ANDA	ANDA203166	LGM PHARMA SOLUTIONS, LLC	NABUMETONE	500 mg/1	100 TABLET, FILM COATED in 1 BOTTLE (79739-7076-1)
15370-170-10	15370-170	HUMAN PRESCRIPTION DRUG	RELAFEN DS	NABUMETONE	TABLET	ORAL	20220512	N/A	ANDA	ANDA203166	Carwin Pharmaceutical Associates, LLC	NABUMETONE	1000 mg/1	100 TABLET in 1 BOTTLE, PLASTIC (15370-170-10)
15370-170-30	15370-170	HUMAN PRESCRIPTION DRUG	RELAFEN DS	NABUMETONE	TABLET	ORAL	20190920	N/A	ANDA	ANDA203166	Carwin Pharmaceutical Associates, LLC	NABUMETONE	1000 mg/1	30 TABLET in 1 BOTTLE, PLASTIC (15370-170-30)
15370-170-60	15370-170	HUMAN PRESCRIPTION DRUG	RELAFEN DS	NABUMETONE	TABLET	ORAL	20200228	N/A	ANDA	ANDA203166	Carwin Pharmaceutical Associates, LLC	NABUMETONE	1000 mg/1	60 TABLET in 1 BOTTLE, PLASTIC (15370-170-60)
15370-170-99	15370-170	HUMAN PRESCRIPTION DRUG	RELAFEN DS	NABUMETONE	TABLET	ORAL	20200228	N/A	ANDA	ANDA203166	Carwin Pharmaceutical Associates, LLC	NABUMETONE	1000 mg/1	1 BLISTER PACK in 1 CARTON (15370-170-99) / 2 TABLET in 1 BLISTER PACK