欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FR/V/0435/001
药品名称
KETASAN 100 MG/ML SOLUTION FOR INJECTION
活性成分
KETAMINE hydrochloride 100.0 mg/ml
剂型
Solution for injection
上市许可持有人
ALFASAN NEDERLAND B.V.
参考成员国 - 产品名称
France (FR)
互认成员国 - 产品名称
Latvia (LV)
Luxembourg (LU)
Lithuania (LT)
Iceland (IS)
Estonia (EE)
Ireland (IE)
Hungary (HU)
Austria (AT)
Bulgaria (BG)
Spain (ES)
Cyprus (CY)
Portugal (PT)
Czechia (CZ)
Italy (IT)
Romania (RO)
Greece (GR)
Slovakia (SK)
Sweden (SE)
Germany (DE)
Slovenia (SI)
Norway (NO)
Denmark (DK)
Ketasan
Croatia (HR)
Finland (FI)
Belgium (BE)
Ketexx Vet 100 mg/ml
United Kingdom (Northern Ireland) (XI)
Poland (PL)
Netherlands (NL)
许可日期
2022/03/30
最近更新日期
2024/10/18
药物ATC编码
QN01AX03 ketamine
申请类型
TypeLevel1:
food
TypeLevel2:
Pharmaceutical
TypeLevel3:
Generic - art 13.2 Dir 2001/82/EC
TypeLevel4:
[not specified]
TypeLevel5:
[not specified]
附件文件下载
PubAR
|
15243 _ Final PuAR
Date of last change:2024/09/06
Final Product Information
|
spc_label_pl_ketexx_d210_clean_final
Date of last change:2024/09/06
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase