欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号DE/H/0015/004
药品名称Actilyse Pulver und Lösungmittel zur Herstellung einer Injektions- bzw. Infusionslösung
活性成分
    • alteplase 1.0 mg/ml
剂型Powder and solvent for solution for injection/infusion
上市许可持有人Boehringer Ingelheim Pharma GmbH & Co.KG Binger Str. 173 55216 Ingelheim Germany
参考成员国 - 产品名称Germany (DE)
互认成员国 - 产品名称
    • Denmark (DK)
    • Belgium (BE)
    • Netherlands (NL)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Finland (FI)
    • Cyprus (CY)
    • Iceland (IS)
    • Malta (MT)
    • Norway (NO)
许可日期2000/12/22
最近更新日期2024/04/18
药物ATC编码
    • B01AD02 alteplase
申请类型
  • TypeLevel1:Line Extension
  • TypeLevel2:Initial Application
  • TypeLevel3:Full Dossier Article 4.8 Di 65/65
  • TypeLevel4:Chemical Substance
  • TypeLevel5:Prescription Only
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市场状态Positive
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