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"
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
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)
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)
47335-712-83 47335-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-712-83)
47335-712-86 47335-712 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (47335-712-86)
47335-711-08 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 (47335-711-08)
47335-711-13 47335-711 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (47335-711-13)
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)
62756-710-08 62756-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-710-08)
62756-710-13 62756-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62756-710-13)
71335-0325-1 71335-0325 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20181127 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71335-0325-1)
71335-0325-2 71335-0325 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20181228 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0325-2)
71335-0325-3 71335-0325 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20181126 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-0325-3)
71335-0325-4 71335-0325 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20220309 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0325-4)
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