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
73473-904-60	73473-904	HUMAN PRESCRIPTION DRUG	brivaracetam	brivaracetam	TABLET, FILM COATED	ORAL	20260204	N/A	ANDA	ANDA214748	Solaris Pharma Corporation	BRIVARACETAM	10 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73473-904-60)
73473-905-60	73473-905	HUMAN PRESCRIPTION DRUG	brivaracetam	brivaracetam	TABLET, FILM COATED	ORAL	20260204	N/A	ANDA	ANDA214748	Solaris Pharma Corporation	BRIVARACETAM	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73473-905-60)
73473-906-60	73473-906	HUMAN PRESCRIPTION DRUG	brivaracetam	brivaracetam	TABLET, FILM COATED	ORAL	20260204	N/A	ANDA	ANDA214748	Solaris Pharma Corporation	BRIVARACETAM	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73473-906-60)
73473-907-60	73473-907	HUMAN PRESCRIPTION DRUG	brivaracetam	brivaracetam	TABLET, FILM COATED	ORAL	20260204	N/A	ANDA	ANDA214748	Solaris Pharma Corporation	BRIVARACETAM	75 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73473-907-60)
73473-908-60	73473-908	HUMAN PRESCRIPTION DRUG	brivaracetam	brivaracetam	TABLET, FILM COATED	ORAL	20260204	N/A	ANDA	ANDA214748	Solaris Pharma Corporation	BRIVARACETAM	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (73473-908-60)