欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0978/002
药品名称
Amlodipine Vitabalans
活性成分
amlodipine 10.0 mg
剂型
Tablet
上市许可持有人
Vitabalans Oy, Finland
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Amlonor 10 mg Tabletten
Denmark (DK)
Norway (NO)
Finland (FI)
Poland (PL)
Amlodipine Vitabalans
Latvia (LV)
Amlodipine Vitabalans 10 mg tabletes
Lithuania (LT)
Amlodipine Vitabalans 10mg tabletės
Estonia (EE)
AMLODIPINE VITABALANS
Hungary (HU)
AMLODIPIN VITABALANS 10 mg tabletta
Czechia (CZ)
Amlodipin Vitabalans 10 mg
Slovakia (SK)
Slovenia (SI)
Iceland (IS)
许可日期
2011/03/16
最近更新日期
2023/02/15
药物ATC编码
C08CA01 amlodipine
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
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
|
SE_H_0978_002_PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase