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
61919-439-60 61919-439 HUMAN PRESCRIPTION DRUG TOPIRAMATE TOPIRAMATE TABLET, FILM COATED ORAL 20190819 N/A ANDA ANDA090278 Direct_Rx TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (61919-439-60)
61919-439-72 61919-439 HUMAN PRESCRIPTION DRUG TOPIRAMATE TOPIRAMATE TABLET, FILM COATED ORAL 20190819 N/A ANDA ANDA090278 Direct_Rx TOPIRAMATE 100 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (61919-439-72)
61919-439-90 61919-439 HUMAN PRESCRIPTION DRUG TOPIRAMATE TOPIRAMATE TABLET, FILM COATED ORAL 20190819 N/A ANDA ANDA090278 Direct_Rx TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (61919-439-90)
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)
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)
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)
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)
70518-1503-0 70518-1503 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20181008 N/A ANDA ANDA090278 REMEDYREPACK INC. TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1503-0)
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)
71335-0548-0 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20210915 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 28 TABLET, FILM COATED in 1 BOTTLE (71335-0548-0)
71335-0548-1 71335-0548 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20180319 N/A ANDA ANDA090278 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (71335-0548-1)
62756-707-08 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (62756-707-08)
62756-707-13 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (62756-707-13)
62756-707-18 62756-707 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA090278 Sun Pharmaceutical Industries, Inc. TOPIRAMATE 25 mg/1 1000 TABLET, FILM COATED in 1 BOTTLE (62756-707-18)
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