欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/7010/001
药品名称Aciclovir 250 mg Powder for solution for infusion
活性成分
    • Aciclovir 250.0 mg
剂型Powder for solution for infusion
上市许可持有人Noridem Enterprises Limited Mitsi Building 3 CY-1065 Nicosia Cyprus
参考成员国 - 产品名称Germany (DE)
Aciclovir Noridem 250 mg Pulver zur Herstellung einer Infusionslösung
互认成员国 - 产品名称
    • Hungary (HU)
    • Ireland (IE)
    • Czechia (CZ)
      Aciclovir Noridem
    • Sweden (SE)
    • Romania (RO)
    • Norway (NO)
    • Slovakia (SK)
    • Finland (FI)
    • Slovenia (SI)
    • Netherlands (NL)
    • Cyprus (CY)
      Aciclovir Noridem 250 mg κόνις για διάλυμα προς έγχυση
    • Croatia (HR)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Denmark (DK)
      Aciclovir Noridem
    • Poland (PL)
      Aciclovir Noridem
    • Belgium (BE)
许可日期2022/11/17
最近更新日期2025/08/15
药物ATC编码
    • J05AB01 aciclovir
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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