欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/0244/002
药品名称
Paroxetin Mylan
活性成分
paroxetine hydrochloride 30.0 mg
剂型
Film-coated tablet
上市许可持有人
Mylan AB Box 230333, 2a 10435 Stockholm Sweden
参考成员国 - 产品名称
Denmark (DK)
互认成员国 - 产品名称
Germany (DE)
Belgium (BE)
Paroxetine Viatris 30 mg FC tablets
Netherlands (NL)
Luxembourg (LU)
United Kingdom (Northern Ireland) (XI)
许可日期
2003/04/25
最近更新日期
2024/04/18
药物ATC编码
N06AB05 paroxetine
申请类型
TypeLevel1:
Line Extension
TypeLevel2:
Initial Application
TypeLevel3:
Generic Article 4.8(a)(iii), first paragraph
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
common-spc-dk0244 clean
Date of last change:2021/08/05
Final Product Information
|
common-spc-dk0244-tracked-v057g[2]
Date of last change:2015/08/05
Final Product Information
|
common-pl-dk0244-30mg-tracked-v057g-rtq[1]
Date of last change:2015/08/05
Final Product Information
|
common-pl-dk0244-20mg-tracked-v057g-rtq[1]
Date of last change:2015/08/05
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase