欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/6027/001
药品名称Sacubitril/Valsartan Synthon 24 mg/26 mg
活性成分
    • Sacubitril sodium 24.3 mg/stuk
    • Valsartan 25.7 mg/stuk
剂型Film-coated tablet
上市许可持有人STADA Arzneimittel AG / DE
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Romania (RO)
      Sacubitril Valsartan STADA 24mg/26mg comprimate filmate
    • Ireland (IE)
    • Slovakia (SK)
      Sacubitril/Valsartan STADA 24 mg/26 mg
    • Austria (AT)
    • Slovenia (SI)
    • France (FR)
    • Malta (MT)
      Sacubitril/Valsartan Clonmel Tablet, film coated 24mg/26mg
    • Spain (ES)
    • Portugal (PT)
    • Greece (GR)
    • Sweden (SE)
    • Germany (DE)
      Sacubitril/Valsartan AL 24 mg/26 mg Filmtabletten
    • Norway (NO)
    • Denmark (DK)
      Sacubitril/Valsartan Stada
    • Finland (FI)
    • Belgium (BE)
    • Hungary (HU)
    • Luxembourg (LU)
    • Cyprus (CY)
      SACUBITRIL+VALSARTAN/STADA 24 mg/26 mg film-coated tablets
    • Iceland (IS)
许可日期2025/06/20
最近更新日期2025/06/21
药物ATC编码
    • C09DX04 valsartan and sacubitril
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Multiple (Copy) 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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