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TEZEFORT

80MG/5MG TBL NOB 14

SÚKL code 0206204
Name of the product TEZEFORT
_MA_MEDICATION_DETAIL_INFO_MED_NAME i TEZEFORT
Supplement 80MG/5MG TBL NOB 14
Strenght 80MG/5MG
Pharmaceutical form Tablet
Package 14
Route Oral use
Language of the pack Czech
Wrap type Blister
Legal status na lékařský předpis
Active substance AMLODIPINE BESILATE (AMLODIPINI BESILAS)
TELMISARTAN (TELMISARTANUM)
ATC group C09DB04
ATC group name TELMISARTAN A AMLODIPIN

Marketing authorisation information

Registration Number 58/ 410/15-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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