欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
SE/H/1119/002
药品名称
Oxycodone Vitabalans
活性成分
oxycodone hydrochloride 10.0 mg
剂型
Film-coated tablet
上市许可持有人
Vitabalance Oy Finland
参考成员国 - 产品名称
Sweden (SE)
互认成员国 - 产品名称
Denmark (DK)
Norway (NO)
Finland (FI)
Poland (PL)
Oxycodone Vitabalans
Latvia (LV)
Lithuania (LT)
Oxycodone Vitabalans 10 mg plėvele dengtos tabletės
Estonia (EE)
OXYCODONE VITABALANS
Hungary (HU)
OXYCODONE VITABALANS 10 mg filmtabletta
Slovenia (SI)
Oksikodon Vitabalans 10 mg filmsko obložene tablete
许可日期
2012/05/03
最近更新日期
2023/06/30
药物ATC编码
N02AA05 oxycodone
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Additional Strength/Form
TypeLevel3:
Generic Art 10.1 and 10.2 Dir 2001/83/EC
TypeLevel4:
Chemical Substance
TypeLevel5:
Prescription Only
附件文件下载
Final PL
|
SE/H/1119/002_Final PL
Date of last change:2014/01/15
Final SPC
|
SE/H/1119/002_Final SPC
Date of last change:2014/01/15
PAR
|
SE/H/1119/002_PAR
Date of last change:2014/01/15
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase