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LORISTA H

100MG/12,5MG TBL FLM 30

SÚKL code 0157779
Name of the product LORISTA H
_MA_MEDICATION_DETAIL_INFO_MED_NAME i LORISTA H
Supplement 100MG/12,5MG TBL FLM 30
Strenght 100MG/12,5MG
Pharmaceutical form Film-coated tablet
Package 30
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance HYDROCHLOROTHIAZIDE (HYDROCHLOROTHIAZIDUM)
LOSARTAN POTASSIUM (LOSARTANUM KALICUM)
ATC group C09DA01
ATC group name LOSARTAN A DIURETIKA
Doping Diuretika a ostatní maskovací látky (nelze pro léčbu sportovců použít vůbec). Bližší informace viz http://www.antidoping.cz/.

Marketing authorisation information

Registration Number 58/ 781/10-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Reference member state
MA status R - active MA/authorised medicinal product
MA Holder Krka, d.d., Novo mesto, Novo mesto
MA Holder country SLOVINSKO

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