欧盟HMA药品数据库（European Union HMA Authorisation of Medicines DataBase）
MR编号
PT/H/1916/001
药品名称
Aciclovir Aurovitas
活性成分
Aciclovir 200.0 mg
剂型
Tablet
上市许可持有人
Generis Phar Unipessoal, Lda.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Spain (ES)
Italy (IT)
许可日期
2019/02/28
最近更新日期
2024/09/16
药物ATC编码
J05AB01 aciclovir
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
|
common_spc_200mg_clean
Date of last change:2024/09/16
PubAR Summary
|
625042_625062_625063_20190411_PAR_GBB
Date of last change:2024/09/06
Final Product Information
|
Labelling_clean
Date of last change:2024/09/06
Final Product Information
|
PIL_200mg_clean
Date of last change:2024/09/06
Final Product Information
|
PIL_400mg_clean
Date of last change:2024/09/06
Final Product Information
|
PIL_800mg_clean
Date of last change:2024/09/06
Final Product Information
|
SPC_200mg _clean
Date of last change:2024/09/06
Final Product Information
|
SPC_400mg_ clean
Date of last change:2024/09/06
Final Product Information
|
SPC_800mg _clean
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase