欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SI/H/0301/001
药品名称Iceland moss herb lozenges
活性成分
    • Iceland moss, dry extract, water (30-40:1) 3.0 mg
剂型Lozenge
上市许可持有人KRKA d.d. Šmarješka cesta 6 8501 Novo mesto
参考成员国 - 产品名称Slovenia (SI)
互认成员国 - 产品名称
    • Iceland (IS)
    • Poland (PL)
    • Latvia (LV)
    • Estonia (EE)
    • Hungary (HU)
      Herbion Iceland 3 mg szopogató tabletta
    • Romania (RO)
      Herbion Iceland pastile
许可日期2024/07/18
最近更新日期2025/01/20
药物ATC编码
    • R05D COUGH SUPPRESSANTS, EXCL. COMBINATIONS WITH EXPECTORANTS
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Article 16a Dir 2001/83/EC
  • TypeLevel4:Herbal
  • TypeLevel5:Non Prescription (including OTC)
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市场状态Positive
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