ALLEGRA

This brand name is authorized in Austria, Brazil, Canada, Croatia, Ecuador, Estonia, Japan, Lithuania, Mexico, Netherlands, Poland, Turkey.

Active ingredients

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

1	Fexofenadine UNII 2S068B75ZU - FEXOFENADINE HYDROCHLORIDE
	Fexofenadine is a non-sedating H1 antihistamine. Fexofenadine is a pharmacologically active metabolite of terfenadine.
	Read more about Fexofenadine

Medication package inserts

Below package inserts are available for further reading:

Document	Type	Information Source
ALLEGRA ALLERGY Film coated tablet	MPI, US: SPL/Old	FDA, National Drug Code (US)

Medicine classification

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

ATC Group		Classification
R06AX26	Fexofenadine	R Respiratory system → R06 Antihistamines for systemic use → R06A Antihistamines for systemic use → R06AX Other antihistamines for systemic use
Discover more medicines within R06AX26

Authorization and marketing

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

Country	Identification scheme	Identifier(s)
BR	Câmara de Regulação do Mercado de Medicamentos	502800405119313, 502800406115311, 502812010059403, 502812010059503, 502812010059603, 502816501139318, 502816502135316, 502818090077403, 576720070076517, 576720080085617, 576720080085717, 576720080085817, 576720080085917, 576720080086017, 576720080086117, 576720100090307, 576720100090407
CA	Health Products and Food Branch	02231462, 02242819
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	29322-08-10, 30127-02-12, 30146-03-12
EE	Ravimiamet	1679654, 1679665, 1679676, 1679687, 1679698, 1679700, 1679711, 1679722, 1679733
HR	Agencija za lijekove i medicinske proizvode	HR-H-986506289
JP	医薬品医療機器総合機構	4490023F1024, 4490023F2020, 4490023R2027
LT	Valstybinė vaistų kontrolės tarnyba	1075662, 1078174, 1078175, 1078176, 1078177, 1078178, 1078179, 1078180, 1078181
MX	Comisión Federal para la Protección contra Riesgos Sanitarios	075M98, 307M2008
NL	Z-Index G-Standaard, PRK	48739
PL	Rejestru Produktów Leczniczych	100086961, 100246608, 100462502
TR	İlaç ve Tıbbi Cihaz Kurumu	8683060090147