欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/7334/001
药品名称Teriflunomid Vivanta Generics 14 mg Filmtabletten
活性成分
    • teriflunomide 14.0 mg
剂型Film-coated tablet
上市许可持有人Vivanta Generics s.r.o. Trtinova 260/1 Cakovice 196 00 Prague Czechia
参考成员国 - 产品名称Germany (DE)
Teriflunomid MSN 14 mg Filmtabletten
互认成员国 - 产品名称
    • Poland (PL)
      Teryflunomid MSN
    • Hungary (HU)
      Teriflunomide MSN 14 mg filmtabletta
    • Bulgaria (BG)
      Teriflunomid MSN
    • Netherlands (NL)
    • Czechia (CZ)
      Teriflunomid MSN
    • Slovenia (SI)
    • Romania (RO)
    • Croatia (HR)
    • Slovakia (SK)
许可日期2023/01/18
最近更新日期2024/09/20
药物ATC编码
    • L04AA31 teriflunomide
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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