欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0640/002
药品名称Ondansetron Kabi 0,08 mg/ml Infusionslösung
活性成分
    • ondansetron hydrochloride 0.08 mg/ml
剂型Solution for infusion
上市许可持有人Fresenius Kabi Deutschland GmbH Else-Kroener-Strasse 1 61352 Bad Homburg Germany
参考成员国 - 产品名称Germany (DE)
Ondansetron Kabi 0,08 mg/ml Infusionslösung
互认成员国 - 产品名称
    • Ireland (IE)
    • Portugal (PT)
    • Spain (ES)
    • Bulgaria (BG)
      Ondansentron Kabi
    • Italy (IT)
    • Cyprus (CY)
      Ondansetron/Kabi 0,08 mg/ml διάλυμα για έγχυση
    • Greece (GR)
    • Croatia (HR)
    • Sweden (SE)
    • Estonia (EE)
    • Norway (NO)
    • Finland (FI)
    • Lithuania (LT)
      Ondansetron Kabi 0,08 mg/ml infuzinis tirpalas
    • Luxembourg (LU)
    • Poland (PL)
      Ondansetron Kabi
    • Romania (RO)
      Ondansetron Kabi 0,08 mg/ml soluție perfuzabilă
    • Hungary (HU)
    • Slovenia (SI)
    • Denmark (DK)
    • Austria (AT)
    • Czechia (CZ)
      Ondansetron Kabi
    • Belgium (BE)
    • Slovakia (SK)
    • Iceland (IS)
    • Netherlands (NL)
    • United Kingdom (Northern Ireland) (XI)
    • Latvia (LV)
许可日期2022/03/03
最近更新日期2024/01/03
药物ATC编码
    • A04AA01 ondansetron
申请类型
  • TypeLevel1:Known Active Substance
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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