欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/0711/001
药品名称
Aridol
活性成分
Mannitol 5.0 mg
Mannitol 0.0 mg
Mannitol 10.0 mg
Mannitol 20.0 mg
Mannitol 40.0 mg
剂型
Inhalation powder, hard capsule
上市许可持有人
Pharmaxis Europe Limited, Ireland
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Germany (DE)
Denmark (DK)
Osmohale
Netherlands (NL)
United Kingdom (Northern Ireland) (XI)
Ireland (IE)
Spain (ES)
Norway (NO)
Finland (FI)
许可日期
2007/05/31
最近更新日期
2024/09/18
药物ATC编码
V04CX Other diagnostic agents
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
Final PL
Final SPC
|
Final SPC
PubAR
|
PAR
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase