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TELMISARTAN/AMLODIPIN TEVA

80MG/5MG TBL NOB 30

SÚKL code 0251736
Name of the product TELMISARTAN/AMLODIPIN TEVA
_MA_MEDICATION_DETAIL_INFO_MED_NAME i TELMISARTAN/AMLODIPIN TEVA
Supplement 80MG/5MG TBL NOB 30
Strenght 80MG/5MG
Pharmaceutical form Tablet
Package 30
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/ 439/20-C
Type of MA A mutual recognition procedure (MRP, DCP), where CZ is Concerned member state
MA status R - active MA/authorised medicinal product
MA Holder Teva B.V., Haarlem
MA Holder country NIZOZEMSKO

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