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"
符合检索条件的记录共 137 条，共 7 页，当前第 4 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
65841-647-16 65841-647 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-647-16)
65841-648-01 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-648-01)
65841-649-01 65841-649 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 100 mg/1 100 TABLET, FILM COATED in 1 BOTTLE (65841-649-01)
65841-649-05 65841-649 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 100 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-649-05)
65841-649-14 65841-649 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 100 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65841-649-14)
65841-649-16 65841-649 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 100 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (65841-649-16)
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)
65841-648-05 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 500 TABLET, FILM COATED in 1 BOTTLE (65841-648-05)
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)
50090-5853-0 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (50090-5853-0)
50090-5853-1 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE (50090-5853-1)
50090-5853-2 50090-5853 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20211110 N/A ANDA ANDA078235 A-S Medication Solutions TOPIRAMATE 25 mg/1 30 TABLET, FILM COATED in 1 BOTTLE (50090-5853-2)
51655-429-26 51655-429 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20230324 N/A ANDA ANDA078235 Northwind Health Company, LLC TOPIRAMATE 25 mg/1 90 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (51655-429-26)
65841-648-14 65841-648 HUMAN PRESCRIPTION DRUG topiramate topiramate TABLET, FILM COATED ORAL 20090327 N/A ANDA ANDA078235 Zydus Lifesciences Limited TOPIRAMATE 50 mg/1 60 TABLET, FILM COATED in 1 BOTTLE (65841-648-14)
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