TOLURA

This brand name is authorized in Albania, Austria, Croatia, Cyprus, Estonia, Finland, France, Germany, Ireland, Italy, Lithuania, Poland, Romania, Singapore, Spain, UK.

Active ingredients

The drug TOLURA contains one active pharmaceutical ingredient (API):

1	Telmisartan UNII U5SYW473RQ - TELMISARTAN
	Telmisartan is an orally active and specific angiotensin II receptor (type AT1) antagonist. Telmisartan selectively binds the AT1 receptor. The binding is long-lasting.
	Read more about Telmisartan

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
TOLURA Tablet	MPI, EU: SmPC	European Medicines Agency (EU)

Medicine classification

This drug has been classified in the anatomical therapeutic chemical (ATC) classification system as follows:

ATC Group		Classification
C09CA07	Telmisartan	C Cardiovascular system → C09 Agents acting on the renin-angiotensin system → C09C Angiotensin II antagonists, plain → C09CA Angiotensin II antagonists, plain
Discover more medicines within C09CA07

Authorization and marketing

This drug has been assigned below unique identifiers within the countries it is being marketed:

Country	Identification scheme	Identifier(s)
AL	Fondi i Sigurimit të Detyrueshëm të Kujdesit Shëndetësor	565/73, 622/73
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	10079787, 10079801, 10079899, 10079907, 10300074, 10300080
EE	Ravimiamet	1482173, 1482184, 1482195, 1482207, 1482218, 1482229, 1482230, 1482241, 1482252, 1482263, 1482274, 1482285, 1482296, 1482308, 1482319, 1482320, 1482331, 1482342, 1482353, 1482364, 1482375, 1664759, 1664760, 1664771
ES	Centro de información online de medicamentos de la AEMPS	110632009, 110632016
FI	Lääkealan turvallisuus- ja kehittämiskeskus	446879, 490670
FR	Base de données publique des médicaments	60798040, 65586116, 68529113
GB	Medicines & Healthcare Products Regulatory Agency	245553, 245555, 245557
IE	Health Products Regulatory Authority	40271, 40288
IT	Agenzia del Farmaco	042284024, 042284099, 042284164
LT	Valstybinė vaistų kontrolės tarnyba	1005606, 1005607, 1055198, 1055199, 1055200, 1055201, 1055202, 1055203, 1055204, 1055205, 1055207, 1055208, 1055209, 1055210, 1055211, 1055212, 1055214, 1055215, 1055216, 1055217, 1055218, 1076192, 1076193, 1076194
PL	Rejestru Produktów Leczniczych	100230820, 100230837, 100230843
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W55585001, W55585002, W55585003, W55585004, W55585005, W55585006, W55585007, W55586001, W55586002, W55586003, W55586004, W55586005, W55586006, W55586007
SG	Health Sciences Authority	15278P, 15279P