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 3 页 ，可点击列名称排序
首页 上一页 下一页 最后一页
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
71335-0548-4 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 56 TABLET, FILM COATED in 1 BOTTLE (71335-0548-4)
71335-0548-5 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20240403 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 84 TABLET, FILM COATED in 1 BOTTLE (71335-0548-5)
71335-0548-6 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20180301 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-0548-6)
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)
62756-710-18 62756-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-710-18)
62756-710-83 62756-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (62756-710-83)
62756-710-86 62756-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (62756-710-86)
62756-710-88 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 (62756-710-88)
63187-801-30 63187-801 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20170102 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (63187-801-30)
63187-801-60 63187-801 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20170102 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (63187-801-60)
63187-801-90 63187-801 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20170102 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (63187-801-90)
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)
70518-0887-0 70518-0887 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20171204 N/A ANDA ANDA090278 REMEDYREPACK INC. TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-0887-0)
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)
商品名称,通用名称,活性成分名称,申请号搜索 高级检索
©2006-2025 Drugfuture->U.S. FDA National Drug Code DataBase