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)
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)
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)
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)
63187-801-30 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)
72789-004-30 72789-004 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190820 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-004-30)
72789-004-60 72789-004 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20200317 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-004-60)
72789-004-21 72789-004 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20190820 N/A ANDA ANDA090278 PD-Rx Pharmaceuticals, Inc. TOPIRAMATE 100 mg/1 21 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (72789-004-21)
71205-819-60 71205-819 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20230703 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (71205-819-60)
71205-819-90 71205-819 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20230703 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71205-819-90)
71205-819-30 71205-819 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20230703 N/A ANDA ANDA090278 Proficient Rx LP TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71205-819-30)
47335-707-13 47335-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (47335-707-13)
47335-707-86 47335-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (47335-707-86)
47335-707-88 47335-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20141215 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (47335-707-88)
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)
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