欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
PT/H/1278/001
药品名称
Levocetirizine Dihydrochloride
活性成分
levocetirizine dihydrochloride 5.0 mg
剂型
Film-coated tablet
上市许可持有人
Activase Pharmaceuticals Limited
参考成员国 - 产品名称
Portugal (PT)
互认成员国 - 产品名称
United Kingdom (Northern Ireland) (XI)
许可日期
2015/06/17
最近更新日期
2023/11/17
药物ATC编码
R06AE09 levocetirizine
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
Final Product Information
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common_interpack
Date of last change:2024/09/06
Final Product Information
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common_pl
Date of last change:2024/09/06
Final Product Information
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common_spc
Date of last change:2024/09/06
PubAR
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PAR
Date of last change:2024/09/06
PubAR Summary
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PAR_summary_generics
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase