欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/0823/002
药品名称Gemcitabine Sandoz 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Sandoz B.V. Veluwezoom 22 1327 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
Gemcitabine Sandoz 1000 mg, poeder voor oplossing voor infusie
互认成员国 - 产品名称
    • Spain (ES)
    • Slovakia (SK)
许可日期2007/08/16
最近更新日期2014/12/15
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
附件文件下载
    市场状态Positive
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