欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号CZ/H/0100/001
药品名称Lorista 50
活性成分
    • losartan potassium salt 50.0 mg
剂型Film-coated tablet
上市许可持有人KRKA d.d. Šmarješka cesta 6, 8501 Novo mesto Slovenia
参考成员国 - 产品名称Czechia (CZ)
互认成员国 - 产品名称
    • Portugal (PT)
    • Hungary (HU)
    • Spain (ES)
    • Norway (NO)
    • Germany (DE)
    • Denmark (DK)
      Losartankalium "Krka"
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Losartan Krka 50 mg Filmtabletten
    • France (FR)
    • Italy (IT)
    • Sweden (SE)
    • Latvia (LV)
    • Bulgaria (BG)
      Lorista
    • Cyprus (CY)
    • Romania (RO)
      Lorista 50 mg comprimate filmate
    • Iceland (IS)
许可日期2005/03/02
最近更新日期2024/07/26
药物ATC编码
    • C09CA01 losartan
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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