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 2 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
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)
43063-997-21 43063-997 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200421 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-21)
43063-997-30 43063-997 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200823 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-30)
43063-997-60 43063-997 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200718 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (43063-997-60)
47335-710-08 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (47335-710-08)
47335-710-13 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (47335-710-13)
47335-710-18 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (47335-710-18)
47335-710-83 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (47335-710-83)
47335-710-86 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (47335-710-86)
47335-710-88 47335-710 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (47335-710-88)
71335-0487-9 71335-0487 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20210915 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-0487-9)
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)
62756-712-88 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 (62756-712-88)
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)
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