欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3313/001
药品名称Gemcitabine SUN
活性成分
    • Gemcitabine hydrochloride 10.0 mg/ml
剂型Solution for infusion
上市许可持有人Sun Pharmaceutical Industries Europe BV
参考成员国 - 产品名称Netherlands (NL)
Gemcitabine SUN 1200/1400/1600/1700/1800/2000/2200 mg oplossing voor infusie
互认成员国 - 产品名称
    • Germany (DE)
      Gemcitabin SUN 10 mg/ml Infusionslösung
    • Denmark (DK)
      Gemcitabin SUN
    • United Kingdom (Northern Ireland) (XI)
    • France (FR)
    • Spain (ES)
    • Italy (IT)
    • Sweden (SE)
    • Norway (NO)
      Gemcitabin Sun
    • Finland (FI)
    • Romania (RO)
      Gemcitabina SUN 10 mg/ml solutie perfuzabila
许可日期2015/09/30
最近更新日期2024/12/03
药物ATC编码
    • L01BC05 gemcitabine
申请类型
  • TypeLevel1:Abridged
  • 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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