欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号NL/V/0343/001
药品名称Apovomin 1 mg/ml solution for injection for dogs
活性成分
    • apomorphine hydrochloride hemihydrate 1.0 mg/ml
剂型Solution for injection
上市许可持有人Dechra Regulatory B.V. Handelsweg 25 5531 AE Bladel Nederland
参考成员国 - 产品名称Netherlands (NL)
Apovomin 1 mg/ml oplossing voor injectie voor honden
互认成员国 - 产品名称
    • United Kingdom (Northern Ireland) (XI)
    • Denmark (DK)
      Apovomin Vet.
    • Iceland (IS)
      Apovomin vet
    • Ireland (IE)
    • Austria (AT)
      Apovomin 1 mg/ml Injektionslösung für Hunde
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
      Apovomin 1 mg/ml šķīdums injekcijām suņiem
    • Lithuania (LT)
    • Estonia (EE)
      Apovomin
    • Hungary (HU)
    • Bulgaria (BG)
    • Czechia (CZ)
      Apovomin 1 mg/ml injekční roztok pro psy
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
许可日期2020/10/21
最近更新日期2021/06/10
药物ATC编码
    • QN04BC07 apomorphine
申请类型
  • TypeLevel1:non-food
  • TypeLevel2:Pharmaceutical
  • TypeLevel3:Full dossier - art 12.3 Dir 2001/82/EC
  • TypeLevel4:[not specified]
  • TypeLevel5:[not specified]
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市场状态Positive
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