欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/4279/004
药品名称Amlodipine besilaat/Valsartan/HCT Sandoz 10 mg/160 mg/25 mg filmomhulde tabletten
活性成分
    • amlodipine 10.0 mg
    • hydrochlorothiazide 25.0 mg
    • valsartan 160.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Amlodipine/Valsartan/HCT Sandoz 10 mg/160 mg/25 mg, filmomhulde tabletten RVG 122470
互认成员国 - 产品名称
    • Germany (DE)
      Amlodipin/Valsartan - 1 A Pharma plus HCT 10 mg/160 mg/25 mg Filmtabletten
    • Austria (AT)
      Amlodipin/Valsartan/HCT Sandoz 10 mg/160 mg/25 mg – Filmtabletten
    • Spain (ES)
    • Greece (GR)
    • Lithuania (LT)
      Dippvol 10 mg/160 mg/25 mg plėvele dengtos tabletės
许可日期2019/05/01
最近更新日期2024/03/19
药物ATC编码
    • C09DX01 valsartan, amlodipine and hydrochlorothiazide
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
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市场状态Positive
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