欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3258/003
药品名称
Mirtazapin Teva B.V.
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-ratiopharm 45 mg Filmtabletten
Luxembourg (LU)
Austria (AT)
Spain (ES)
Finland (FI)
许可日期
2023/03/09
最近更新日期
2024/12/17
药物ATC编码
N06AX11 mirtazapine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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 PL
|
mirtazapine_dk_h_3258_3262_3263_001_003_pil_10_07_24
Date of last change:2024/10/21
Final Labelling
|
Common LAB_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