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
80425-0398-1 80425-0398 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20240604 N/A ANDA ANDA078235 Advanced Rx of Tennessee, LLC TOPIRAMATE 100 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (80425-0398-1)
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)
65841-650-01 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)
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)
50090-5309-2 50090-5309 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20201028 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5309-2)
50090-5309-3 50090-5309 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20220310 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 100 mg/1 180 TABLET, FILM COATED in 1 BOTTLE (50090-5309-3)
51655-746-26 51655-746 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20230105 N/A ANDA ANDA078235 Northwind Health Company, LLC TOPIRAMATE 50 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-26)
51655-746-52 51655-746 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20221230 N/A ANDA ANDA078235 Northwind Health Company, LLC TOPIRAMATE 50 mg/1 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-746-52)
68382-141-14 68382-141 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 200 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (68382-141-14)
68382-141-16 68382-141 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Pharmaceuticals USA Inc. TOPIRAMATE 200 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (68382-141-16)
80425-0398-2 80425-0398 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20240604 N/A ANDA ANDA078235 Advanced Rx of Tennessee, LLC TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (80425-0398-2)
80425-0398-3 80425-0398 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20240604 N/A ANDA ANDA078235 Advanced Rx of Tennessee, LLC TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (80425-0398-3)
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