欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0722/003
药品名称XEOMIN 200 Einheiten Pulver zur Herstellung einer Injektionslösung
活性成分
    • Clostridium botulinum type A neurotoxin complex 200.0 LD50 units
剂型Powder for solution for injection
上市许可持有人Merz Pharmaceuticals GmbH Eckenheimer Landstr. 100 60318 Frankfurt am Main Germany
参考成员国 - 产品名称Germany (DE)
Xeomin
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
      XEOMEEN 200 unités poudre pour solution injectable
    • Netherlands (NL)
    • Luxembourg (LU)
    • Iceland (IS)
    • Ireland (IE)
    • Liechtenstein (LI)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
      XEOMIN
    • Sweden (SE)
    • Norway (NO)
      Xeomin
    • Finland (FI)
    • Poland (PL)
      Xeomin
    • Latvia (LV)
      Xeomin 200 V pulveris injekciju šķīduma pagatavošanai
    • Lithuania (LT)
      XEOMIN 200 V milteliai injekciniam tirpalui
    • Estonia (EE)
    • Hungary (HU)
      XEOMIN 200 egység por oldatos injekcióhoz
    • Bulgaria (BG)
      XEOMIN
    • Cyprus (CY)
    • Czechia (CZ)
      XEOMIN 200 jednotek prášek pro injekční roztok
    • Romania (RO)
      XEOMIN 200 unităţi pulbere pentru soluţie injectabilă
    • Slovakia (SK)
      XEOMIN 200 LD50 jednotiek prášok na injekčný roztok
    • Slovenia (SI)
    • Malta (MT)
      XEOMIN 200 LD50 units powder for solution for injection
    • Croatia (HR)
许可日期2016/04/05
最近更新日期2024/12/09
药物ATC编码
    • M03AX01 botulinum toxin
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Art 8.3(i) 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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