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=NDA020505"
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
50458-639-65 50458-639 HUMAN PRESCRIPTION DRUG Topamax topiramate TABLET, COATED ORAL 19970101 N/A NDA NDA020505 Janssen Pharmaceuticals, Inc. TOPIRAMATE 25 mg/1 60 TABLET, COATED in 1 BOTTLE (50458-639-65)
50458-640-65 50458-640 HUMAN PRESCRIPTION DRUG Topamax topiramate TABLET, COATED ORAL 19970101 N/A NDA NDA020505 Janssen Pharmaceuticals, Inc. TOPIRAMATE 50 mg/1 60 TABLET, COATED in 1 BOTTLE (50458-640-65)
50458-641-65 50458-641 HUMAN PRESCRIPTION DRUG Topamax topiramate TABLET, COATED ORAL 19970101 N/A NDA NDA020505 Janssen Pharmaceuticals, Inc. TOPIRAMATE 100 mg/1 60 TABLET, COATED in 1 BOTTLE (50458-641-65)
50458-642-65 50458-642 HUMAN PRESCRIPTION DRUG Topamax topiramate TABLET, COATED ORAL 19970101 N/A NDA NDA020505 Janssen Pharmaceuticals, Inc. TOPIRAMATE 200 mg/1 60 TABLET, COATED in 1 BOTTLE (50458-642-65)
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