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=ANDA090278"
符合检索条件的记录共 103 条，共 6 页，当前第 4 页 ，可点击列名称排序
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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
47335-711-18 47335-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (47335-711-18)
47335-711-83 47335-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-711-83)
47335-711-86 47335-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (47335-711-86)
47335-711-88 47335-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (47335-711-88)
68071-5165-6 68071-5165 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200205 N/A ANDA ANDA090278 NuCare Pharmaceuticals,Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68071-5165-6)
62756-711-08 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-711-08)
62756-711-13 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62756-711-13)
62756-711-18 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-711-18)
62756-711-83 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62756-711-83)
62756-711-86 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (62756-711-86)
62756-711-88 62756-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-711-88)
71335-0487-5 71335-0487 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-0487-5)
71335-0487-6 71335-0487 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 80 TABLET, FILM COATED in 1 BOTTLE (71335-0487-6)
71335-0487-7 71335-0487 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20221010 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0487-7)
71205-214-30 71205-214 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-214-30)
71205-214-60 71205-214 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-214-60)
71205-214-90 71205-214 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190201 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-214-90)
62756-707-08 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-707-08)
62756-707-13 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62756-707-13)
62756-707-18 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-707-18)
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