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=ANDA204511"
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
35208-031-10 35208-031 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-release Levetiracetam TABLET, EXTENDED RELEASE ORAL 20161003 N/A ANDA ANDA204511 IntelliPharmaCeutics Corp. LEVETIRACETAM 500 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (35208-031-10)
35208-031-60 35208-031 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-release Levetiracetam TABLET, EXTENDED RELEASE ORAL 20161003 N/A ANDA ANDA204511 IntelliPharmaCeutics Corp. LEVETIRACETAM 500 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (35208-031-60)
35208-032-10 35208-032 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-release Levetiracetam TABLET, EXTENDED RELEASE ORAL 20161003 N/A ANDA ANDA204511 IntelliPharmaCeutics Corp. LEVETIRACETAM 750 mg/1 1000 TABLET, EXTENDED RELEASE in 1 BOTTLE (35208-032-10)
35208-032-60 35208-032 HUMAN PRESCRIPTION DRUG Levetiracetam Extended-release Levetiracetam TABLET, EXTENDED RELEASE ORAL 20161003 N/A ANDA ANDA204511 IntelliPharmaCeutics Corp. LEVETIRACETAM 750 mg/1 60 TABLET, EXTENDED RELEASE in 1 BOTTLE (35208-032-60)
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