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
80425-0092-2	80425-0092	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA078235	Advanced Rx Pharmacy of Tennessee, LLC	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0092-2)
80425-0398-1	80425-0398	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20240604	N/A	ANDA	ANDA078235	Advanced Rx of Tennessee, LLC	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE (80425-0398-1)
80425-0398-2	80425-0398	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20240604	N/A	ANDA	ANDA078235	Advanced Rx of Tennessee, LLC	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (80425-0398-2)
80425-0398-3	80425-0398	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20240604	N/A	ANDA	ANDA078235	Advanced Rx of Tennessee, LLC	TOPIRAMATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE (80425-0398-3)
82009-135-05	82009-135	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230724	N/A	ANDA	ANDA078235	Quallent Pharmaceuticals Health LLC	TOPIRAMATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-135-05)
82009-136-05	82009-136	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230724	N/A	ANDA	ANDA078235	Quallent Pharmaceuticals Health LLC	TOPIRAMATE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-136-05)
82009-137-05	82009-137	HUMAN PRESCRIPTION DRUG	topiramate	topiramate	TABLET, FILM COATED	ORAL	20230724	N/A	ANDA	ANDA078235	Quallent Pharmaceuticals Health LLC	TOPIRAMATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (82009-137-05)