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
68462-108-60	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)
0615-8139-39	0615-8139	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181207	N/A	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)
68462-153-05	68462-153	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	50 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-153-05)
68462-153-10	68462-153	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	50 mg/1	1000 TABLET, FILM COATED in 1 BOTTLE (68462-153-10)
68462-153-60	68462-153	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20090327	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	50 mg/1	60 TABLET, FILM COATED in 1 BOTTLE (68462-153-60)
0615-8140-39	0615-8140	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20181220	N/A	ANDA	ANDA077627	NCS HealthCare of KY, LLC dba Vangard Labs	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8140-39)
51655-608-26	51655-608	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077627	Northwind Pharmaceuticals, LLC	TOPIRAMATE	100 mg/1	90 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-608-26)
51655-608-52	51655-608	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20150202	N/A	ANDA	ANDA077627	Northwind Pharmaceuticals, LLC	TOPIRAMATE	100 mg/1	30 TABLET, FILM COATED in 1 BOTTLE, DISPENSING (51655-608-52)
68462-109-05	68462-109	HUMAN PRESCRIPTION DRUG	Topiramate	Topiramate	TABLET, FILM COATED	ORAL	20200730	N/A	ANDA	ANDA077627	Glenmark Pharmaceuticals Inc., USA	TOPIRAMATE	100 mg/1	500 TABLET, FILM COATED in 1 BOTTLE (68462-109-05)
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)