欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/H/0239/002
药品名称
MYFORTIC 360mg
活性成分
[No Active-Substance specified] 0.0 -
剂型
Gastro-resistant tablet
上市许可持有人
Novartis Pharma SAS
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Slovakia (SK)
Slovenia (SI)
Estonia (EE)
Czechia (CZ)
Germany (DE)
Denmark (DK)
Belgium (BE)
Netherlands (NL)
Luxembourg (LU)
Iceland (IS)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Austria (AT)
Myfortic 360 mg - magensaftresistente Filmtabletten
Spain (ES)
Portugal (PT)
Latvia (LV)
Italy (IT)
Lithuania (LT)
Greece (GR)
Hungary (HU)
Sweden (SE)
Cyprus (CY)
Norway (NO)
Malta (MT)
Finland (FI)
Poland (PL)
许可日期
2004/02/07
最近更新日期
2025/02/07
药物ATC编码
L04AA06 mycophenolic acid
申请类型
TypeLevel1:
New Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Article 4.8 Di 65/65
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final SPC
|
common_combined_PI_Myfortic_360_with clean_corrected
Date of last change:2024/11/22
Final Product Information
|
common_combined_PI_Myfortic_180_with clean_corrected
Date of last change:2024/11/22
Final PL
|
Myfortic PI 360mg_marked FINAL Draft_Ib42
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase