欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号NL/V/0241/001
药品名称Laxatract 667 mg/ml oral solution
活性成分
    • lactulose 667.0 mg/ml
剂型Oral liquid
上市许可持有人Dechra Regulatory B.V.
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)
      Laxatract 667 mg/ml
    • Luxembourg (LU)
    • Iceland (IS)
      Laxatract 667 mg/ml saft handa hundum og köttum
    • Ireland (IE)
    • Austria (AT)
      Laxatract 667 mg/ml Sirup für Hunde und Katzen
    • France (FR)
      LAXATRACT 667 MG/ML SOLUTION BUVABLE POUR CHIENS ET CHATS
    • Spain (ES)
    • Portugal (PT)
    • Italy (IT)
    • Greece (GR)
    • Sweden (SE)
    • Norway (NO)
      Laxatract
    • Finland (FI)
    • Poland (PL)
    • Latvia (LV)
    • Lithuania (LT)
    • Estonia (EE)
      Laxatract
    • Hungary (HU)
    • Bulgaria (BG)
    • Cyprus (CY)
    • Czechia (CZ)
      Laxatract 667 mg/ml sirup pro psy a kočky
    • Romania (RO)
    • Slovakia (SK)
    • Slovenia (SI)
    • Croatia (HR)
    • United Kingdom (Northern Ireland) (XI)
许可日期2018/10/23
最近更新日期2021/04/23
药物ATC编码
    • QA06AD11 lactulose
申请类型
  • TypeLevel1：non-food
  • TypeLevel2：Pharmaceutical
  • TypeLevel3：Generic - art 13.2 Dir 2001/82/EC
  • TypeLevel4：[not specified]
  • TypeLevel5：[not specified]
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市场状态Positive
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