欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号SE/H/0229/004
药品名称Symbicort
活性成分
    • Budesonide 80.0 µg/dose
    • Formoterol fumarate 2.25 µg/dose
剂型Pressurised inhalation, suspension
上市许可持有人AstraZeneca AB, Sweden
参考成员国 - 产品名称Sweden (SE)
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      Symbicort 80 microgram/2,25 microgram/inhalatie, aërosol, suspensie
    • Netherlands (NL)
      Symbicort aërosol 100/3, 100 microgram / 3 microgram per dosis, aërosol, suspensie
    • Luxembourg (LU)
    • Iceland (IS)
      Symbicort 80/2,25 míkróg/skammt Innúðalyf, dreifa
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Norway (NO)
      Symbicort
    • Finland (FI)
    • Latvia (LV)
      Symbicort 80 mikrogrami/2,25 mikrogrami/izsmidzinājumā, aerosols inhalācijām, zem spiediena, suspensija
    • Lithuania (LT)
      Symbicort Turbuhaler 80 mikrogramų/2,25 mikrogramo/išpurškime suslėgtoji įkvepiamoji suspensija
    • Estonia (EE)
      SYMBICORT
    • Hungary (HU)
      SYMBICORT 2,25 mikrogramm/80 mikrogramm/adag túlnyomásos inhalációs szuszpenzió
    • Cyprus (CY)
    • Czechia (CZ)
      Symbicort 80 mikrogramů/2,25 mikrogramu suspenze k inhalaci v tlakovém obalu
    • Romania (RO)
      Symbicort 80 micrograme/2,25 micrograme/inhalaţie, suspensie de inhalat presurizată
    • Slovakia (SK)
    • Slovenia (SI)
    • Malta (MT)
    • Croatia (HR)
      Symbicort 80 mikrograma/2,25 mikrograma po potisku, stlačeni inhalat, suspenzija
    • United Kingdom (Northern Ireland) (XI)
许可日期2020/05/18
最近更新日期2024/12/02
药物ATC编码
    • R03AK07 formoterol and budesonide
申请类型
  • TypeLevel1:Line Extension
  • TypeLevel2:Additional Strength/Form
  • TypeLevel3:Fixed combination Art 10b 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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