ACEBUTOLOL AUROVITAS

400MG TBL FLM 100

SÚKL code 0220435
Name of the product ACEBUTOLOL AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ACEBUTOLOL AUROVITAS
Supplement 400MG TBL FLM 100
Strenght 400MG
Pharmaceutical form Film-coated tablet
Package 100
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ACEBUTOLOL HYDROCHLORIDE (ACEBUTOLOLI HYDROCHLORIDUM)
ATC group C07AB04
ATC group name ACEBUTOLOL
Doping Alkohol (zakázán pouze při soutěži v určitých sportech). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 58/ 963/16-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 30. 04. 2020
MA Holder Aurovitas Pharma Polska Sp. z o.o., Warszawa
MA Holder country POLSKO
Actual MA holder Aurovitas, spol. s r.o., Praha
Actual MA holder country ČESKÁ REPUBLIKA

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