欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/0487/006
药品名称
Olanzapina Aurobindo
活性成分
olanzapine 20.0 mg
剂型
Tablet
上市许可持有人
Aurobindo Pharma (Malta) Ltd, Malta
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Belgium (BE)
Finland (FI)
Malta (MT)
Olanzapine Tablets 20mg
Germany (DE)
Olanzapin Aurobindo 20 mg, Tabletten
Netherlands (NL)
Romania (RO)
Olanzapina Aurobindo 20 mg comprimate
许可日期
2011/11/03
最近更新日期
2024/08/09
药物ATC编码
N05AH03 olanzapine
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
|
52532_52533_52535_52538_52539_20120217_52540_PAR_JLE
Date of last change:2024/09/06
Final Product Information
|
52550_52552_52555_52556_52557_52558_20120217_PAR_JLE
Date of last change:2024/09/06
Final PL
|
common_pl
Date of last change:2024/09/06
Final SPC
|
common_spc
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase