欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/3775/001
药品名称Cymevene 500 mg, powder for concentrate for solution for infusion.
活性成分
    • ganciclovir 500.0 mg
剂型Powder for concentrate for solution for injection/infusion
上市许可持有人CHEPLAPHARM Arzneimittel GmbH Ziegelhof 24 17489 Greifswald Duitsland
参考成员国 - 产品名称Netherlands (NL)
Cymevene 500 mg, poeder voor concentraat voor oplossing voor infusie
互认成员国 - 产品名称
    • Sweden (SE)
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
    • France (FR)
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Norway (NO)
    • Finland (FI)
    • Poland (PL)
    • Hungary (HU)
    • Czechia (CZ)
    • Slovakia (SK)
    • Croatia (HR)
许可日期2016/05/12
最近更新日期2023/05/12
药物ATC编码
    • J05AB06 ganciclovir
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：[not specified]
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
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市场状态Positive
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