NEBIVOLOL AUROVITAS

5MG TBL NOB 250

SÚKL code 0173757
Name of the product NEBIVOLOL AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i NEBIVOLOL AUROVITAS
Supplement 5MG TBL NOB 250
Strenght 5MG
Pharmaceutical form Tablet
Package 250
Route Oral use
Language of the pack Czech
Wrap type Tablet container
Legal status na lékařský předpis
Active substance NEBIVOLOL HYDROCHLORIDE (NEBIVOLOLI HYDROCHLORIDUM)
ATC group C07AB12
ATC group name NEBIVOLOL
Doping Alkohol (zakázán pouze při soutěži v určitých sportech). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 77/ 853/16-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 31. 10. 2018
MA Holder Aurovitas, Unipessoal, Lda., Carnaxide
MA Holder country PORTUGALSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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