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EPIRUBICIN ACTAVIS

2MG/ML INJ SOL 1X25ML II

SÚKL code 0224653
Name of the product EPIRUBICIN ACTAVIS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i EPIRUBICIN ACTAVIS
Supplement 2MG/ML INJ SOL 1X25ML II
Strenght 2MG/ML
Pharmaceutical form Solution for injection
Package 1X25ML II
Route Intravenous/intravesical use
Language of the pack Czech
Wrap type Vial
Legal status na lékařský předpis
Active substance EPIRUBICIN HYDROCHLORIDE (EPIRUBICINI HYDROCHLORIDUM)
ATC group L01DB03
ATC group name EPIRUBICIN

Marketing authorisation information

Registration Number 44/ 108/08-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Reference member state
MA status B - medicinal product after change, may be placed on the market for the period of 6 months (Placed on the market till) and used until expiration, not later than till the end of validity of the marketing authorisation (Valid till)
Placed on the market till 31. 12. 2022
MA Holder Actavis Group PTC ehf., Hafnarfjördur
MA Holder country ISLAND
Actual MA holder Teva B.V., Haarlem
Actual MA holder country NIZOZEMSKO

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