欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1732/004
药品名称Zoloft 20 mg/ml
活性成分
    • sertraline 20.0 mg/ml
剂型Oral solution
上市许可持有人Pfizer BV Capelle a/d IJssel The Netherlands MRP-product following art 30 referral
参考成员国 - 产品名称Netherlands (NL)
互认成员国 - 产品名称
    • Finland (FI)
    • Poland (PL)
    • Germany (DE)
    • Spain (ES)
    • Belgium (BE)
    • Portugal (PT)
    • Italy (IT)
    • Sweden (SE)
    • Hungary (HU)
      ZOLOFT 20 mg/ml koncentrátum belsőleges oldathoz
    • Romania (RO)
      Zoloft 20 mg/ml concentrat pentru soluţie orală
    • Slovenia (SI)
    • Slovakia (SK)
    • Luxembourg (LU)
    • Iceland (IS)
    • Norway (NO)
许可日期2009/12/15
最近更新日期2024/07/18
药物ATC编码
    • N06AB06 sertraline
申请类型
  • TypeLevel1：[not specified]
  • TypeLevel2：[not specified]
  • TypeLevel3：[not specified]
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
附件文件下载
市场状态Positive
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