欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
DK/H/3362/001
药品名称
Suprane
活性成分
Desflurane 100.0 % (V/V)
剂型
Inhalation vapour, liquid
上市许可持有人
Baxter A/S Tobaksvejen 23A 2860 Søborg Denmark
参考成员国 - 产品名称
Denmark (DK)
Suprane
互认成员国 - 产品名称
Hungary (HU)
Suprane folyadék inhalációs gőz képzéséhez
Bulgaria (BG)
Suprane
Czechia (CZ)
SUPRANE 100% tekutina k inhalaci parou
Iceland (IS)
Romania (RO)
Suprane 100% vapori de inhalat, lichid
Spain (ES)
Slovakia (SK)
Sweden (SE)
Slovenia (SI)
Norway (NO)
Malta (MT)
Suprane 100% Inhalation vapour, solution
Finland (FI)
Desflurane Baxter
Croatia (HR)
Latvia (LV)
Lithuania (LT)
Suprane 100% įkvepiamieji garai, skystis
Estonia (EE)
许可日期
2022/10/03
最近更新日期
2025/04/14
药物ATC编码
N01AB07 desflurane
申请类型
TypeLevel1:
Known Active Substance
TypeLevel2:
Initial Application
TypeLevel3:
Full Dossier Art 8.3(i) Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final Labelling
|
common_interpack_supranemrp_0010
Date of last change:2024/09/06
Final SPC
|
common_spc_2023_03_delirium_suprane_c
Date of last change:2024/09/06
Final PL
|
DK_H_3362_001_IB_005_common_PL_final_clean
Date of last change:2024/09/06
PubAR
|
PAR_Scientific discussion
Date of last change:2024/09/06
PubAR Summary
|
Summary PAR
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase