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 106 条，共 6 页，当前第 5 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
71335-0548-7 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20180423 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-0548-7)
71335-0548-8 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190123 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-0548-8)
71335-0548-9 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-0548-9)
62756-712-08 62756-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-712-08)
62756-712-13 62756-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62756-712-13)
62756-712-18 62756-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-712-18)
62756-712-83 62756-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62756-712-83)
62756-712-86 62756-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (62756-712-86)
71335-0925-2 71335-0925 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20180810 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0925-2)
71335-0925-3 71335-0925 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240404 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0925-3)
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)
63187-060-30 63187-060 HUMAN PRESCRIPTION DRUG TOPIRAMATE TOPIRAMATE TABLET, FILM COATED ORAL 20190101 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-060-30)
47335-712-08 47335-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (47335-712-08)
47335-712-13 47335-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (47335-712-13)
47335-712-18 47335-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (47335-712-18)
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