欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/H/1732/002
药品名称Zoloft 50
活性成分
    • sertraline 50.0 mg
剂型Film-coated tablet
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
    • Germany (DE)
    • Denmark (DK)
    • Belgium (BE)
    • Luxembourg (LU)
    • Iceland (IS)
    • United Kingdom (Northern Ireland) (XI)
    • Ireland (IE)
    • Austria (AT)
      Tresleen 50 mg - Filmtabletten
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
    • Finland (FI)
    • Bulgaria (BG)
      Zoloft
    • Cyprus (CY)
    • Czechia (CZ)
    • Estonia (EE)
    • Hungary (HU)
      ZOLOFT 50 mg filmtabletta
    • Lithuania (LT)
      Zoloft 50 mg plėvele dengtos tabletės
    • Latvia (LV)
      Zoloft 50 mg apvalkotās tabletes
    • Poland (PL)
      Zoloft
    • Romania (RO)
      Zoloft 50 mg comprimate filmate
    • Slovenia (SI)
    • Slovakia (SK)
许可日期2009/09/28
最近更新日期2024/02/13
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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