欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/1162/002
药品名称Gemcitabine "Ebewe" 1000 mg
活性成分
    • gemcitabine hydrochloride 1000.0 mg
剂型Powder for solution for infusion
上市许可持有人Ebewe Pharma GmbH Nfg. KG Mondseestrasse 11, 4866 Unternach Austria
参考成员国 - 产品名称Netherlands (NL)
Gemcitabine "Ebewe" 1000 mg poeder voor oplossing voor infusie
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Spain (ES)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Lithuania (LT)
    • Bulgaria (BG)
    • Romania (RO)
    • Slovakia (SK)
    • Malta (MT)
许可日期2008/07/01
最近更新日期2020/01/27
药物ATC编码
    • L01BC05 gemcitabine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Additional Strength/Form
  • 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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