欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/4407/001
药品名称Biorphen 0,1 mg/ml Injektions-/Infusionslösung
活性成分
    • PHENYLEPHRINE HYDROCHLORIDE 0.1 mg/ml
剂型Solution for injection/infusion
上市许可持有人Sintetica GmbH Albersloher Weg 11 48155 Münster Germany
参考成员国 - 产品名称Germany (DE)
Biorphen 0.1 mg/ml Infusionslösung
互认成员国 - 产品名称
    • Austria (AT)
      Biorphen 0,1 mg/ml Infusionslösung
    • Cyprus (CY)
      Biorphen 0.1mg/ml Solution for Infusion
    • Denmark (DK)
    • Estonia (EE)
      BIORPHEN
    • Greece (GR)
    • Finland (FI)
    • Croatia (HR)
      Biorphen 0,1 mg/ml otopina za injekciju/infuziju
    • Hungary (HU)
      BIORPHEN 0,1 mg/ml oldatos injekció vagy infúzió
    • Iceland (IS)
    • Latvia (LV)
      Biorphen 0,1 mg/ml šķīdums injekcijām/infūzijām
    • Lithuania (LT)
      Phenylephrine hydrochloride Sintetica 0,1 mg/ml injekcinis ar infuzinis tirpalas
    • Netherlands (NL)
    • Norway (NO)
    • Poland (PL)
      Biorphen
    • Romania (RO)
      Biorphen 0.1 mg/ml solutie perfuzabila
    • Sweden (SE)
    • Slovenia (SI)
许可日期2016/09/19
最近更新日期2023/12/13
药物ATC编码
    • C01CA06 phenylephrine
申请类型
  • TypeLevel1:Abridged
  • TypeLevel2:Initial Application
  • TypeLevel3:Other Generic application Art 10.3 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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