欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DE/H/6968/002
药品名称Gemcitabine SUN 1 g Pulver zur Herstellung einer Infusionslösung
活性成分
    • gemcitabine hydrochloride 1.0 g
剂型Powder for solution for infusion
上市许可持有人Sun Pharmaceuticals Germany GmbH Hemmelrather Weg 201, Gebäude GIZ 1 51377 Leverkusen Germany
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Netherlands (NL)
    • Spain (ES)
    • Italy (IT)
    • United Kingdom (Northern Ireland) (XI)
    • Romania (RO)
      Gemcitabină Sun 1 g, pulbere pentru soluţie perfuzabilă
许可日期2008/04/22
最近更新日期2024/02/13
药物ATC编码
    • L01BC05 gemcitabine
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：[not specified]
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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