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=ANDA078235"
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
71335-1147-3 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190314 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (71335-1147-3)
71335-1147-4 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200204 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE (71335-1147-4)
71335-1147-5 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200803 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 7 TABLET, FILM COATED in 1 BOTTLE (71335-1147-5)
71335-1147-6 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20220502 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 80 TABLET, FILM COATED in 1 BOTTLE (71335-1147-6)
71335-1147-7 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20201102 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1147-7)
71335-1147-8 71335-1147 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20220502 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 50 mg/1 45 TABLET, FILM COATED in 1 BOTTLE (71335-1147-8)
71335-1684-8 71335-1684 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20200910 N/A ANDA ANDA078235 Bryant Ranch Prepack TOPIRAMATE 25 mg/1 14 TABLET, FILM COATED in 1 BOTTLE (71335-1684-8)
65841-650-01 65841-650 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 200 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-650-01)
68071-4877-3 68071-4877 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190501 N/A ANDA ANDA078235 NuCare Pharmaceuticals,Inc. TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (68071-4877-3)
68084-344-01 68084-344 HUMAN PRESCRIPTION DRUG Topiramate Topiramate TABLET, FILM COATED ORAL 20090421 N/A ANDA ANDA078235 American Health Packaging TOPIRAMATE 100 mg/1 100 BLISTER PACK in 1 BOX, UNIT-DOSE (68084-344-01) / 1 TABLET, FILM COATED in 1 BLISTER PACK (68084-344-11)
70518-1937-0 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20190306 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BLISTER PACK (70518-1937-0)
70518-1937-3 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20210707 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 100 POUCH in 1 BOX (70518-1937-3) / 1 TABLET, FILM COATED in 1 POUCH (70518-1937-4)
70518-1937-5 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20240408 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-5)
70518-1937-6 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20250701 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 180 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-6)
70518-1937-7 70518-1937 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20260316 N/A ANDA ANDA078235 REMEDYREPACK INC. TOPIRAMATE 50 mg/1 120 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (70518-1937-7)
65841-650-05 65841-650 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 200 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-650-05)
65841-650-14 65841-650 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65841-650-14)
65841-650-16 65841-650 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-650-16)
50090-5309-0 50090-5309 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20201028 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5309-0)
50090-5309-1 50090-5309 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20201028 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5309-1)
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