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)
检索条件:" 注册申请号=ANDA077627"
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
43063-605-30 43063-605 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20150831 N/A ANDA ANDA077627 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-605-30)
43063-612-30 43063-612 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20151008 N/A ANDA ANDA077627 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-612-30)
43063-612-60 43063-612 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20151008 N/A ANDA ANDA077627 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-612-60)
0615-8138-39 0615-8138 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20180709 N/A ANDA ANDA077627 NCS HealthCare of KY, LLC dba Vangard Labs TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (0615-8138-39)
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)
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)
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)
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)
68462-110-05 68462-110 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200730 N/A ANDA ANDA077627 Glenmark Pharmaceuticals Inc., USA TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (68462-110-05)
68462-110-10 68462-110 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA077627 Glenmark Pharmaceuticals Inc., USA TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (68462-110-10)
68462-110-60 68462-110 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA077627 Glenmark Pharmaceuticals Inc., USA TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68462-110-60)
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)
70518-2899-0 70518-2899 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200930 N/A ANDA ANDA077627 REMEDYREPACK INC. TOPIRAMATE 25 mg/1 30 POUCH in 1 BOX (70518-2899-0) / 1 TABLET, FILM COATED in 1 POUCH (70518-2899-1)
63187-118-90 63187-118 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA077627 Proficient Rx LP TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-118-90)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2024 Drugfuture->U.S. FDA National Drug Code DataBase