IFIRMASTA

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

Active ingredients

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

1	Irbesartan UNII J0E2756Z7N - IRBESARTAN
	Irbesartan is a potent, orally active, selective angiotensin-II receptor (type AT1) antagonist. It is expected to block all actions of angiotensin-II mediated by the AT1 receptor, regardless of the source or route of synthesis of angiotensin-II. The selective antagonism of the angiotensin-II (AT1) receptors results in increases in plasma renin levels and angiotensin-II levels, and a decrease in plasma aldosterone concentration.
	Read more about Irbesartan

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
IFIRMASTA Film-coated 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
C09CA04	Irbesartan	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 C09CA04

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	366/73, 367/73
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	09726342, 09726359, 09726365, 09726371, 09726388, 09726394, 09726402, 09726419, 09726425
EE	Ravimiamet	1391868, 1391879, 1391880, 1391891, 1391903, 1391914, 1391925, 1391936, 1391947, 1391958, 1391969, 1391970, 1391981, 1391992, 1392005, 1598531, 1598542, 1598553, 1598564, 1598575, 1598586
ES	Centro de información online de medicamentos de la AEMPS	08480002, 08480008, 08480014
FR	Base de données publique des médicaments	60488216, 60582498, 66542998
GB	Medicines & Healthcare Products Regulatory Agency	227204, 227207, 227209
IE	Health Products Regulatory Authority	54317, 54318, 54319
IT	Agenzia del Farmaco	041666088, 041666140
LT	Valstybinė vaistų kontrolės tarnyba	1035185, 1035186, 1035187, 1035188, 1035189, 1035190, 1035191, 1035192, 1035193, 1035194, 1035195, 1035196, 1035198, 1035199, 1035200, 1035201, 1035202, 1035203, 1069774, 1069775, 1069776, 1069777, 1069778, 1069779
PL	Rejestru Produktów Leczniczych	100310677, 100310690, 100310720
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W55941001, W55941002, W55941003, W55941004, W55941005, W55941006, W55942001, W55942002, W55942003, W55942004, W55942005, W55942006, W55943001, W55943002, W55943003, W55943004, W55943005, W55943006