ESCITALOPRAM FARMAX

10MG TBL FLM 30

SÚKL code 0170585
Name of the product ESCITALOPRAM FARMAX 10 MG POTAHOVANÉ TABLETY
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ESCITALOPRAM FARMAX
Supplement 10MG TBL FLM 30
Strenght 10MG
Pharmaceutical form Film-coated tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ESCITALOPRAM OXALATE (ESCITALOPRAMI OXALAS)
ATC group N06AB10
ATC group name ESCITALOPRAM

Marketing authorisation information

Registration Number 30/ 641/11-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned 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 30. 04. 2019
MA Holder SVUS Pharma a.s., Hradec Králové
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder Neuraxpharm Bohemia s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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