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ALFUZOSIN AUROVITAS

10MG TBL PRO 90

SÚKL code 0235020
Name of the product ALFUZOSIN AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ALFUZOSIN AUROVITAS
Supplement 10MG TBL PRO 90
Strenght 10MG
Pharmaceutical form Prolonged-release tablet
Package 90
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance ALFUZOSIN HYDROCHLORIDE (ALFUZOSINI HYDROCHLORIDUM)
ATC group G04CA01
ATC group name ALFUZOSIN

Marketing authorisation information

Registration Number 77/ 214/14-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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