欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号DK/H/1217/001
药品名称Fluvastatin "Actavis"
活性成分
    • fluvastatin 80.0 mg
剂型Prolonged-release tablet
上市许可持有人Splitting prcedure: New split procedure number is UK/H/6827/001 (UK) and PT/H/2038/001 (PT, DE, IT, NL) Actavis Group PTC ehf, Reykjavikurvegur 76-78, IS-220 Hafnarfjördur, Iceland
参考成员国 - 产品名称Denmark (DK)
Fluvastatin "Actavis"
互认成员国 - 产品名称
    • Germany (DE)
    • Netherlands (NL)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Portugal (PT)
    • Italy (IT)
许可日期2008/06/12
最近更新日期2019/05/24
药物ATC编码
    • C10AA04 fluvastatin
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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