欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号PT/H/0703/002
药品名称Venlafaxina Aurobindo
活性成分
    • venlafaxine hydrochloride 75.0 mg
剂型Prolonged-release capsule, hard
上市许可持有人Aurobindo Pharma (Portugal), Unip, Lda.
参考成员国 - 产品名称Portugal (PT)
互认成员国 - 产品名称
    • Germany (DE)
      Venlafaxine Aurobindo 75 mg Hartkapsel, retadiert
    • Netherlands (NL)
      Venlafaxine Aurobindo 75 mg, capsules met verlengde afgifte, hard
    • Ireland (IE)
    • France (FR)
    • Italy (IT)
    • Poland (PL)
      Venlafaxine Aurobindo
    • Malta (MT)
      Venlafaxine Aurobindo 75mg prolonged-release capsules, hard
许可日期2014/12/18
最近更新日期2023/09/15
药物ATC编码
    • N06AX16 venlafaxine
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
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