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
71335-0325-7	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20220309	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-0325-7)
71335-0325-8	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20190523	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0325-8)
71335-0548-9	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	45 TABLET, FILM COATED in 1 BOTTLE (71335-0548-9)
71335-0325-1	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181127	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (71335-0325-1)
71335-0325-2	71335-0325	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181228	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (71335-0325-2)