BETAXOLOL XANTIS

20MG TBL NOB 30

SÚKL code 0249444
Name of the product BETAXOLOL XANTIS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i BETAXOLOL XANTIS
Supplement 20MG TBL NOB 30
Strenght 20MG
Pharmaceutical form Tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance BETAXOLOL HYDROCHLORIDE (BETAXOLOLI HYDROCHLORIDUM)
ATC group C07AB05
ATC group name BETAXOLOL
Doping Alkohol (zakázán pouze při soutěži v určitých sportech). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 58/ 024/17-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 30. 04. 2021
MA Holder MEDREG s.r.o., Praha
MA Holder country ČESKÁ REPUBLIKA
Actual MA holder MEDREG s.r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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