欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号CZ/H/0101/001
药品名称Lorista H 50 mg/12,5 mg
活性成分
    • Hydrochlorothiazide 25.0 mg
    • Losartan potassium salt 100.0 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)
215182/10
互认成员国 - 产品名称
    • Iceland (IS)
    • Germany (DE)
    • Denmark (DK)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Losartan/HCT Krka 50 mg/12,5 mg Filmtabletten
    • Italy (IT)
    • Sweden (SE)
    • Latvia (LV)
    • Portugal (PT)
    • Cyprus (CY)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
      Lorista H
    • Estonia (EE)
      LORISTA H
    • Hungary (HU)
    • Slovakia (SK)
    • Lithuania (LT)
许可日期2005/03/02
最近更新日期2025/09/05
药物ATC编码
    • C09DA01 losartan and diuretics
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic [Article 10.1.(a)(iii), first paragraph]
  • TypeLevel4：Chemical Substance
  • TypeLevel5：Prescription Only
附件文件下载
市场状态Positive
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase