欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1422/002
药品名称Omeprazol CF 20mg
活性成分
    • omeprazole 20.0 mg
剂型Gastro-resistant capsule*
上市许可持有人Centrafarm BV Nieuwe Donk 3 4879 AC Etten-Leur The Netherlands
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Austria (AT)
      Omeprazol STADA 20 mg magensaftresistente Hartkapseln
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Finland (FI)
    • Latvia (LV)
      Omeprazole STADA 20 mg zarnās šķīstošās cietās kapsulas
    • Lithuania (LT)
      Omeprazole STADA 20 mg skrandyje neirios kietos kapsulės
    • Estonia (EE)
      OMEPRAZOLE STADA 20 MG
    • Czechia (CZ)
    • Slovakia (SK)
许可日期2008/12/20
最近更新日期2023/10/12
药物ATC编码
    • A02BC01 omeprazole
申请类型
  • TypeLevel1：Abridged
  • TypeLevel2：Initial Application
  • TypeLevel3：Generic Art 10.1 and 10.2 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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