欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NO/H/0999/001
药品名称Zolpidem tartrate
活性成分
    • zolpidem tartrate 5.0 mg
    • zolpidem tartrate 10.0 mg
剂型Film-coated tablet
上市许可持有人Sanofi-aventis Recherche & Développement 1, Avenue Pierre Brossolette – 91380 Chilly Mazarin – France
参考成员国 - 产品名称Norway (NO)
互认成员国 - 产品名称
    • Romania (RO)
    • Slovakia (SK)
    • Germany (DE)
    • Belgium (BE)
    • Malta (MT)
    • Denmark (DK)
    • Sweden (SE)
    • Luxembourg (LU)
    • France (FR)
    • Spain (ES)
    • Austria (AT)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Iceland (IS)
    • Poland (PL)
    • Ireland (IE)
    • Latvia (LV)
    • Finland (FI)
    • Lithuania (LT)
    • Estonia (EE)
    • Hungary (HU)
    • Cyprus (CY)
    • Czechia (CZ)
许可日期2015/05/06
最近更新日期2024/08/30
药物ATC编码
    • N05CF02 zolpidem
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Repeat Use
  • TypeLevel3:Informed Consent Art 10c Dir 2001/83/EC
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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    市场状态Positive
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