欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0703/001
药品名称
Venlafaxina Aurobindo
活性成分
venlafaxine hydrochloride 37.5 mg
剂型
Prolonged-release capsule, hard
上市许可持有人
Aurobindo Pharma (Portugal), Unip, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Malta (MT)
Venlafaxine Aurobindo 37.5mg prolonged-release capsules, hard
Germany (DE)
Venlafaxine Aurobindo 37,5 mg Hartkapsel, retardiert
Netherlands (NL)
Venlafaxine Aurobindo 37,5 mg, capsules met verlengde afgifte, hard
France (FR)
Italy (IT)
Poland (PL)
Venlafaxine Aurobindo
许可日期
2014/12/18
最近更新日期
2023/09/15
药物ATC编码
N06AX16 venlafaxine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial 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 Product Information
|
common-pl-clean
Date of last change:2015/10/09
Final Product Information
|
common-spc-clean
Date of last change:2015/10/09
Final Product Information
|
common-outer
Date of last change:2015/10/09
PAR
|
54238_54239_54240_20150211_PAR_GBB
Date of last change:2015/10/09
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase