欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0204/001
药品名称Ranitidin Actavis
活性成分
    • ranitidine hydrochloride 150.0 mg
剂型Film-coated tablet
上市许可持有人Split procedure: New procedure no is PT/H/2184/01 Actavis Group PTC ehf, Island
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    许可日期2000/09/07
    最近更新日期2019/03/29
    药物ATC编码
      • A02BA02 ranitidine
    申请类型
    • TypeLevel1:Abridged
    • TypeLevel2:Initial Application
    • TypeLevel3:Generic Article 4.8(a)(iii), first paragraph
    • TypeLevel4:Chemical Substance
    • TypeLevel5:Prescription Only
    附件文件下载
    市场状态Withdrawn(注:已撤市)
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