欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0382/001
药品名称Teveten Plus HCT 600 mg/12,5 mg
活性成分
    • eprosartan mesilate 735.8 mg
    • hydrochlorothiazide 12.5 mg
剂型Film-coated tablet
上市许可持有人Viatris Healthcare GmbH Lütticher Straße 5 53842 Troisdorf Germany
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Belgium (BE)
    • Luxembourg (LU)
    • Ireland (IE)
    • Austria (AT)
      Teveten Plus 600 mg/12,5 mg Filmtabletten
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
许可日期2004/05/24
最近更新日期2024/02/13
药物ATC编码
    • C09DA02 eprosartan and diuretics
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Fixed Combination Article 4.8b
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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