欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0356/002
药品名称
Certican
活性成分
Everolimus 0.5 mg
剂型
Tablet
上市许可持有人
Novartis Sverige AB Sweden
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Belgium (BE)
Luxembourg (LU)
Iceland (IS)
Austria (AT)
Certican 0,5 mg - Tabletten
France (FR)
Spain (ES)
Portugal (PT)
Italy (IT)
Greece (GR)
Norway (NO)
Finland (FI)
Poland (PL)
Lithuania (LT)
Certican 0,5mg tabletės
Estonia (EE)
Hungary (HU)
Slovenia (SI)
Bulgaria (BG)
Certican
Romania (RO)
CERTICAN 0,50 mg comprimate
Croatia (HR)
许可日期
2003/12/02
最近更新日期
2025/09/22
药物ATC编码
L04AA18 everolimus
申请类型
TypeLevel1:
New Active Substance
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Full Dossier Article 4.8 Di 65/65
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
Final PL
Final SPC
|
Final SPC
PubAR
|
PAR
PubAR Summary
|
PAR Summary
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase