欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/6021/001
药品名称Raltegravir Viatris 600 mg Film-Coated Tablets
活性成分
    • Raltegravir potassium 600.0 mg
剂型Film-coated tablet
上市许可持有人Viatris Limited Damastown Industrial Park Mulhuddart D15XD71 Dublin Ireland
参考成员国 - 产品名称Netherlands (NL)
Raltegravir Viatris 600 mg, filmomhulde tabletten
互认成员国 - 产品名称
    • Latvia (LV)
    • Estonia (EE)
    • Germany (DE)
    • Bulgaria (BG)
      Raltegavir Vale
    • Denmark (DK)
      Raltegravir Viatris
    • Cyprus (CY)
      Raltegravir Vale 600 mg επικαλυμμένα με λεπτό υμένιο δισκία
    • France (FR)
    • Romania (RO)
      Raltegravir Vale 600 mg comprimate filmate
    • Spain (ES)
    • Malta (MT)
      Raltegravir Vale 600 mg film-coated tablets
    • Portugal (PT)
    • Croatia (HR)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
      Raltegravir Viatris
    • Finland (FI)
    • Poland (PL)
      Raltegravir Vale
许可日期2025/04/09
最近更新日期2025/06/19
药物ATC编码
    • J05AJ01 raltegravir
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Generic Art 10.1 and 10.2 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
附件文件下载
    市场状态Positive
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