欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1192/002
药品名称
Aciclovir Hikma
活性成分
Aciclovir 500.0 mg
剂型
Powder for solution for infusion
上市许可持有人
Hikma Farmacêutica (Portugal), S.A.
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
Germany (DE)
Aciclovir Hikma 500 mg Pulver zur Herstellung einer Infusionslösung
Italy (IT)
Belgium (BE)
Aciclovir Hikma 500 mg poudre pour solution pour perfusion
United Kingdom (Northern Ireland) (XI)
France (FR)
Poland (PL)
Aciclovir Hikma
Netherlands (NL)
Austria (AT)
许可日期
2014/10/14
最近更新日期
2025/01/20
药物ATC编码
J05AB01 aciclovir
申请类型
TypeLevel1:
Known Active Substance
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
PubAR
|
579720_579721_20150424_PAR_RCM
Date of last change:2024/09/06
Final Product Information
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common_impack_aciclovir
Date of last change:2024/09/06
Final Product Information
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common_outer_aciclovir_clean
Date of last change:2024/09/06
Final Labelling
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common_outer_allstrengthsmar15 _tracked_
Date of last change:2024/09/06
Final Product Information
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common_pl_aciclovir_clean
Date of last change:2024/09/06
Final PL
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common_pl_allstrengthsmar15 _tracked_
Date of last change:2024/09/06
Final Product Information
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common_spc_aciclovir_clean
Date of last change:2024/09/06
Final SPC
|
common_spc_allstrengthsmar15 _tracked_
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase