欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3262/003
药品名称
Mirtazapin Teva
活性成分
mirtazapine 45.0 mg
剂型
Film-coated tablet
上市许可持有人
Teva B.V. Swensweg 5 2031GA Haarlem Netherlands
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Germany (DE)
Mirtazapin AbZ 45 mg Filmtabletten
Netherlands (NL)
Mirtazapine Teva 45 mg, filmomhulde tabletten
Iceland (IS)
Austria (AT)
Portugal (PT)
许可日期
2023/03/09
最近更新日期
2023/11/23
药物ATC编码
N06AX11 mirtazapine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Multiple (Copy) 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
Final Labelling
|
Common LAB_Mirtazapine
Date of last change:2024/09/06
Final PL
|
Common PL_Mirtazapine
Date of last change:2024/09/06
Final SPC
|
Common SPC_Mirtazapine
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase