ILIBRIFT

7,5MG TBL FLM 14

SÚKL code 0223469
Name of the product ILIBRIFT
_MA_MEDICATION_DETAIL_INFO_MED_NAME i ILIBRIFT
Supplement 7,5MG TBL FLM 14
Strenght 7,5MG
Pharmaceutical form Film-coated tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance IVABRADINE HYDROCHLORIDE (IVABRADINI HYDROCHLORIDUM)
ATC group C01EB17
ATC group name IVABRADIN

Marketing authorisation information

Registration Number 41/ 831/15-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 Zentiva, k.s., Praha
MA Holder country ČESKÁ REPUBLIKA

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