DUTASTERID/TAMSULOSIN AUROVITAS

0,5MG/0,4MG CPS DUR 90

SÚKL code 0228818
Name of the product DUTASTERID/TAMSULOSIN AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i DUTASTERID/TAMSULOSIN AUROVITAS
Supplement 0,5MG/0,4MG CPS DUR 90
Strenght 0,5MG/0,4MG
Pharmaceutical form Capsule, hard
Package 90
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance TAMSULOSIN HYDROCHLORIDE (TAMSULOSINI HYDROCHLORIDUM)
DUTASTERIDE (DUTASTERIDUM)
ATC group G04CA52
ATC group name TAMSULOSIN A DUTASTERID

Marketing authorisation information

Registration Number 87/ 165/18-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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