欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号IS/H/0469/001
药品名称Teriflunomid Zentiva
活性成分
    • Teriflunomide 14.0 mg
剂型Film-coated tablet
上市许可持有人Zentiva, k. s. U kabelovny 130, 102 37 Praha 10 - Dolní Měcholupy, Česká republika
参考成员国 - 产品名称Iceland (IS)
Teriflunomid Zentiva
互认成员国 - 产品名称
    • Bulgaria (BG)
    • France (FR)
    • Czechia (CZ)
      Teriflunomid Zentiva
    • Spain (ES)
    • Romania (RO)
      Teriflunomida Zentiva 14mg, comprimate filmate
    • Portugal (PT)
    • Slovakia (SK)
    • Italy (IT)
    • Croatia (HR)
    • Sweden (SE)
    • Norway (NO)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
      Teriflunomide Zentiva 14 mg plėvele dengtos tabletės
    • Germany (DE)
      Teriflunomid Zentiva 14 mg Filmtabletten
    • Estonia (EE)
    • Denmark (DK)
    • Hungary (HU)
      Teriflunomide Zentiva 14 mg filmtabletta
    • Austria (AT)
许可日期2023/01/05
最近更新日期2025/09/05
药物ATC编码
    • L04AA31 teriflunomide
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
©2006-2025 Drugfuture->European Union HMA Authorisation of Medicines DataBase