欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/2617/004
药品名称Candesartan-HCTad 32 mg / 25 mg Tabletten
活性成分
    • candesartancilexetil 32.0 mg
    • hydrochlorothiazide 25.0 mg
剂型Tablet
上市许可持有人KRKA d.d. Novo mesto Smarjeska cesta 6 8501 Novo mesto Slovenia
参考成员国 - 产品名称Germany (DE)
Candesartan HCT C 32/25 mg Tabletten
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
      Candesartan cilexetil HCTZ Krka 32 mg/25 mg tabletten
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Candecombi 32 mg/25 mg Tabletten
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
      Candesartan/Hydrochlorothiazide Krka
    • Finland (FI)
许可日期2011/02/18
最近更新日期2024/01/15
药物ATC编码
    • C09DA06 candesartan and diuretics
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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
©2006-2024 Drugfuture->European Union HMA Authorisation of Medicines DataBase