欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0803/001
药品名称Nebivolol 5 mg
活性成分
    • nebivolol 5.0 mg
剂型Tablet
上市许可持有人Centrafarm Services B.V. Nieuwe Donk 9 NL-4879 AC Etten-Leur The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
      Nebivolol STADA 5 mg Tabletten
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Nebovolol STADA 5 mg -Tabletten
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Latvia (LV)
      Nemirostad 5 mg tablets
    • Lithuania (LT)
      NEMIROSTAD 5 mg tabletės
    • Estonia (EE)
      NEBILOSTAD
许可日期2007/03/15
最近更新日期2023/10/12
药物ATC编码
    • C07AB12 nebivolol
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
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市场状态Positive
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