欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号IS/H/0571/001
药品名称Dimethyl fumarate Teva
活性成分
    • dimethyl fumarate 120.0 mg
剂型Gastro-resistant capsule, hard
上市许可持有人Teva GmbH Graf-Arco-Str. 3 89079, Ulm, Germany
参考成员国 - 产品名称Iceland (IS)
Damperit
互认成员国 - 产品名称
    • Hungary (HU)
      Damperit 120 mg gyomornedv-ellenálló kemény kapszula
    • Spain (ES)
    • Cyprus (CY)
      Damperit 120 gastro-resistant capsules, hard
    • Portugal (PT)
    • Czechia (CZ)
      DAMPERIT
    • Italy (IT)
    • Slovakia (SK)
    • Greece (GR)
    • Slovenia (SI)
    • Sweden (SE)
    • Croatia (HR)
    • Germany (DE)
      DAMPERIT 120 mg magensaftresistente Hartkapseln
    • Norway (NO)
    • Denmark (DK)
      Dimethyl fumarate Teva
    • Finland (FI)
    • Belgium (BE)
      Dimethyl Fumarate rtp 120 mg harde maagsapresistente capsules
    • Poland (PL)
      Damperit
    • Netherlands (NL)
      Dimethylfumaraat Teva 120 mg, harde maagsapresistente capsules
    • Latvia (LV)
    • Ireland (IE)
    • Lithuania (LT)
      Dimethyl fumarate Teva 120 mg skrandyje neirios kietosios kapsulės
    • Austria (AT)
    • Estonia (EE)
    • France (FR)
许可日期2024/12/02
最近更新日期2025/05/05
药物ATC编码
    • L04AX07 dimethyl fumarate
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
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市场状态Positive
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