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
71335-0548-4	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	56 TABLET, FILM COATED in 1 BOTTLE (71335-0548-4)
71335-0548-5	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20240403	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	84 TABLET, FILM COATED in 1 BOTTLE (71335-0548-5)
71335-0548-6	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180301	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	120 TABLET, FILM COATED in 1 BOTTLE (71335-0548-6)
71335-0548-7	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20180423	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	7 TABLET, FILM COATED in 1 BOTTLE (71335-0548-7)
71335-0548-8	71335-0548	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20190123	N/A	ANDA	ANDA090278	Bryant Ranch Prepack	TOPIRAMATE	25 mg/1	14 TABLET, FILM COATED in 1 BOTTLE (71335-0548-8)
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)