欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0642/002
药品名称
Atorvastatin Krka
活性成分
Atorvastatin calcium salt 20.0 mg
剂型
Film-coated tablet
上市许可持有人
Krka Sverige AB, Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Belgium (BE)
Atorvastatin HCS 20 mg filmomhulde tabletten
Italy (IT)
Greece (GR)
Cyprus (CY)
Romania (RO)
Atoris 20 mg comprimate filmate
Iceland (IS)
Denmark (DK)
Austria (AT)
Atorvastatin KRKA 20 mg Filmtabletten
Norway (NO)
Finland (FI)
Germany (DE)
许可日期
2008/03/13
最近更新日期
2025/01/15
药物ATC编码
C10AA05 atorvastatin
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 PL
|
SE_H_0642_002_Final PL
Date of last change:2024/09/06
Final SPC
|
SE_H_0642_002_Final SPC
Date of last change:2024/09/06
PubAR
|
SE_H_0642_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