欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SK/H/0156/001
药品名称Duloxetine Krka 30 mg hard gastro-resistant capsules
活性成分
    • Duloxetine 30.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Krka, d.d., Novo mesto Šmarješka cesta 6 8501 Novo meto, Slovenia
参考成员国 - 产品名称Slovakia (SK)
Duloxetin Krka 30 mg tvrdé gastrorezistentné kapsuly
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Duloxetine KRKA 30 mg maagsapresistente capsules, hard
    • Netherlands (NL)
    • Iceland (IS)
      Duloxetin Krka 30 mg Magasýruþolið hart hylki
    • Ireland (IE)
    • Austria (AT)
      Duloxetin Krka 30 mg magensaftresistente Hartkapseln
    • Sweden (SE)
    • Norway (NO)
      Duloxetin Krka
    • Finland (FI)
许可日期2015/02/17
最近更新日期2024/09/10
药物ATC编码
    • N06AX21 duloxetine
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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