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
68462-109-10	68462-109	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	100 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-109-10)
68462-109-60	68462-109	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	100 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68462-109-60)
0615-8139-39	0615-8139	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181207	20260630	ANDA	ANDA077627	NCS HealthCare of KY, LLC dba Vangard Labs	TOPIRAMATE	50 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8139-39)
70518-4340-0	70518-4340	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20250515	N/A	ANDA	ANDA077627	REMEDYREPACK INC.	TOPIRAMATE	50 mg/1	100 POUCH in 1 BOX (70518-4340-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-4340-1)
70518-4340-2	70518-4340	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20250609	N/A	ANDA	ANDA077627	REMEDYREPACK INC.	TOPIRAMATE	50 mg/1	30 POUCH in 1 BOX (70518-4340-2) / 1 TABLET, FILM COATED in 1 POUCH (70518-4340-3)
68462-108-05	68462-108	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	25 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-108-05)
68462-108-10	68462-108	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	25 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-108-10)
68462-108-60	68462-108	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	25 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68462-108-60)