欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号ES/H/0857/005
药品名称Amlodipine/Valsartan/HCTZ Krka
活性成分
    • amlodipine besilate 10.0 mg
    • hydrochlorothiazide 25.0 mg
    • valsartan 320.0 mg
剂型Film-coated tablet
上市许可持有人Krka d.d. Novo mesto Šmarješka cesta 6 Novo mesto 8501 Slovenia
参考成员国 - 产品名称Spain (ES)
互认成员国 - 产品名称
    • Iceland (IS)
    • Czechia (CZ)
      Amlodipine/Valsartan/HCTZ Krka
    • Denmark (DK)
    • Belgium (BE)
      Amlodipine/Valsartan/Hydrochlorothiazide Krka 10 mg/320 mg/25 mg filmomhulde tabletten
    • Greece (GR)
    • Norway (NO)
      Amlodipine/Valsartan/Hydrochlorothiazide Krka
    • Finland (FI)
    • Portugal (PT)
    • Ireland (IE)
许可日期2019/01/22
最近更新日期2023/09/22
药物ATC编码
    • C09DX01 valsartan, amlodipine and hydrochlorothiazide
申请类型
  • TypeLevel1:[not specified]
  • TypeLevel2:[not specified]
  • TypeLevel3:[not specified]
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
附件文件下载
市场状态Positive
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