欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1041/002
药品名称
Valtrex
活性成分
valaciclovir hydrochloride 500.0 mg
剂型
Film-coated tablet
上市许可持有人
GlaxoSmithKline AB, Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Portugal (PT)
Netherlands (NL)
Austria (AT)
Valtrex 500 mg - Filmtabletten
Belgium (BE)
Bulgaria (BG)
Valtrex
Cyprus (CY)
Czechia (CZ)
Germany (DE)
Greece (GR)
Spain (ES)
Finland (FI)
France (FR)
Ireland (IE)
Iceland (IS)
Italy (IT)
Lithuania (LT)
Valtrex 500 mg plėvele dengtos tabletės
Luxembourg (LU)
Latvia (LV)
Norway (NO)
Romania (RO)
Valtrex 500 mg comprimate filmate
Slovenia (SI)
Slovakia (SK)
Estonia (EE)
许可日期
2010/08/09
最近更新日期
2024/03/15
药物ATC编码
J05AB11 valaciclovir
申请类型
TypeLevel1:
[not specified]
TypeLevel2:
[not specified]
TypeLevel3:
[not specified]
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
Final PL
|
SE/H/1041/002_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/1041/002_Final SPC
Date of last change:2014/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase