HYDROCHLOROTHIAZIDE AUROVITAS

25MG TBL NOB 90

SÚKL code 0228279
Name of the product HYDROCHLOROTHIAZIDE AUROVITAS
_MA_MEDICATION_DETAIL_INFO_MED_NAME i HYDROCHLOROTHIAZIDE AUROVITAS
Supplement 25MG TBL NOB 90
Strenght 25MG
Pharmaceutical form Tablet
Package 90
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDUM)
ATC group C03AA03
ATC group name HYDROCHLOROTHIAZID
Doping Diuretika a ostatní maskovací látky (nelze pro léčbu sportovců použít vůbec). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 50/ 043/18-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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