欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0505/002
药品名称
VENLAFAXINE SUN LP
活性成分
Venlafaxine hydrochloride 75.0 mg
剂型
Prolonged-release capsule*
上市许可持有人
SUN PHARMA FRANCE
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
许可日期
2012/06/13
最近更新日期
2024/11/05
药物ATC编码
N06AX16 venlafaxine
N06A ANTIDEPRESSANTS
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 SPC
|
20120820_fr505_VenlafaxineRanbaxy_par_pdf
Date of last change:2024/09/06
PubAR
|
20120820_fr505_VenlafaxineRanbaxy_par_pdf_2
Date of last change:2024/09/06
Final SPC
|
20120820_fr505_VenlafaxineRanbaxy_pl_pdf
Date of last change:2024/09/06
Final Product Information
|
20120820_fr505_VenlafaxineRanbaxy_pl_pdf_2
Date of last change:2024/09/06
Final SPC
|
20120820_fr505_VenlafaxineRanbaxy_spc_pdf
Date of last change:2024/09/06
Final Product Information
|
20120820_fr505_VenlafaxineRanbaxy_spc_pdf_2
Date of last change:2024/09/06
市场状态
Withdrawn(注:已撤市)
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