欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/H/2151/002
药品名称Levetiracetam 500 mg Film-coated tablet
活性成分
    • Levetiracetam 500.0 mg
剂型Film-coated tablet
上市许可持有人Sandoz B.V. Veluwezoom 22 1327 AH Almere P.O. box 10332 1301 AH Almere The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Denmark (DK)
      Levetriacetam "Sandoz"
    • Belgium (BE)
    • United Kingdom (Northern Ireland) (XI)
    • Austria (AT)
      Levetiracetam Sandoz 500 mg - Filmtabletten
    • France (FR)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
      Levetiracetam Sandoz
    • Norway (NO)
    • Finland (FI)
    • Hungary (HU)
      LEVETIRACETAM SANDOZ 500 mg filmtabletta
    • Slovakia (SK)
    • Spain (ES)
许可日期2011/08/29
最近更新日期2025/01/24
药物ATC编码
    • N03AX14 levetiracetam
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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