欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4298/002
药品名称Amlodipin/Valsartan AL 5 mg/ 160 mg Filmtabletten
活性成分
    • AMLODIPINE BESILATE 6.93 mg
    • valsartan 160.0 mg
剂型Film-coated tablet
上市许可持有人ALIUD PHARMA GmbH Gottlieb-Daimler-Str. 19 89150 Laichingen Germany
参考成员国 - 产品名称Germany (DE)
Amlodipin/Valsartan AL 5 mg/160 mg Filmtabletten
互认成员国 - 产品名称
    • Sweden (SE)
    • Finland (FI)
    • Romania (RO)
      Amlodipină/Valsartan STADA 5 mg/160 mg comprimate filmate
    • Denmark (DK)
    • Belgium (BE)
      Amlodipine/Valsartan EG 5 mg/160 mg filmomhulde tabletten
    • Luxembourg (LU)
      Amlodipine/Valsartan EG, 5 mg / 160 mg, Comprimé pelliculé
    • Ireland (IE)
    • Austria (AT)
      Amlodipin/Valsartan STADA 5 mg/160 mg Filmtabletten
    • Spain (ES)
    • Portugal (PT)
许可日期2016/04/11
最近更新日期2024/07/23
药物ATC编码
    • C09DB01 valsartan and amlodipine
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • 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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