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=ANDA078235"
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
68788-7351-9 68788-7351 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190227 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7351-9)
68788-7351-5 68788-7351 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190227 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 50 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7351-5)
68788-7351-6 68788-7351 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190227 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7351-6)
68788-7351-1 68788-7351 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190227 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (68788-7351-1)
68788-7460-3 68788-7460 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7460-3)
68788-7460-9 68788-7460 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7460-9)
68788-7468-3 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7468-3)
68788-7468-5 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7468-5)
68788-7468-6 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7468-6)
68788-7468-9 68788-7468 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200302 N/A ANDA ANDA078235 Preferred Pharmaceuticals Inc. TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7468-9)
68788-7460-5 68788-7460 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7460-5)
68788-7460-6 68788-7460 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7460-6)
68788-7460-8 68788-7460 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20210921 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (68788-7460-8)
68788-7568-3 68788-7568 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68788-7568-3)
68788-7568-5 68788-7568 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 200 mg/1 15 TABLET, FILM COATED in 1 BOTTLE (68788-7568-5)
68788-7568-6 68788-7568 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68788-7568-6)
68788-7568-9 68788-7568 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20191227 N/A ANDA ANDA078235 Preferred Pharmaceuticals, Inc. TOPIRAMATE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68788-7568-9)
65841-647-01 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-647-01)
65841-648-01 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-648-01)
65841-648-05 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-648-05)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2026 Drugfuture->U.S. FDA National Drug Code DataBase