欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/3297/002
药品名称Dulodet 60 mg gastroresistant capsules, hard
活性成分
    • Duloxetine 30.0 mg
剂型Capsule, hard
上市许可持有人Egis Pharmaceuticals PLC H-1106 Budapest Keresztúri út 30-38 HUNGARY
参考成员国 - 产品名称Netherlands (NL)
Dulodet 60 mg harde maagsapresistente capsules
互认成员国 - 产品名称
    • Hungary (HU)
      DULODET 60 mg gyomornedv-ellenálló kemény kapszula
    • Bulgaria (BG)
      Duloxetin PI Ltd.
许可日期2015/07/23
最近更新日期2024/11/13
药物ATC编码
    • N06AX21 duloxetine
申请类型
  • TypeLevel1:Known Active Substance
  • 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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