欧盟HMA药品数据库(European Union HMA Authorisation of Medicines DataBase)
MR编号
FI/H/1142/003
药品名称
Carbidopa/Levodopa Orion 25/250 mg
活性成分
Carbidopa 25.0 mg
Levodopa 250.0 mg
剂型
Tablet
上市许可持有人
Orion Corporation Orionintie 1 02200 ESPOO Finland
参考成员国 - 产品名称
Finland (FI)
互认成员国 - 产品名称
Romania (RO)
Slovakia (SK)
Belgium (BE)
Slovenia (SI)
France (FR)
Croatia (HR)
Spain (ES)
Italy (IT)
Poland (PL)
Parkador
Latvia (LV)
Lithuania (LT)
Levodopa/Carbidopa Orion 250 mg/25 mg tabletės
Estonia (EE)
Bulgaria (BG)
PARKADOR
Czechia (CZ)
PIPODA
许可日期
2024/04/03
最近更新日期
2025/02/10
药物ATC编码
N04BA02 levodopa and decarboxylase inhibitor
申请类型
TypeLevel1:
Abridged
TypeLevel2:
Initial Application
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
|
EU Carbidopa_Levodopa Orion 25_250 25_100 12_5_50 tabl PIL 241224
Date of last change:2025/06/06
Final SPC
|
EU Carbidopa Levodopa Orion 25_250 25_100 12_5_50 tabl SPC 080224
Date of last change:2025/04/29
Final Labelling
|
EU Carbidopa_Levodopa Orion 25_250 25_100 12_5_50 tabl LABEL 080224
Date of last change:2025/04/29
PubAR
|
Carbidopa_Levodopa Orion FI_H_1142_003_DC PAR
Date of last change:2025/04/29
市场状态
Positive
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European Union HMA Authorisation of Medicines DataBase