TELFAST

This brand name is authorized in Australia, Croatia, Cyprus, Finland, France, Germany, Hong Kong SAR China, Ireland, Italy, Malta, Netherlands, New Zealand, Poland, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

The drug TELFAST 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
TELFAST Film-coated tablet	MPI, EU: SmPC	Health Products Regulatory Authority (IE)

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)
AU	Pharmaceutical Benefits Scheme	4237B, 4238C
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00018520, 00018537, 00018543, 01229638, 01229644, 01229650, 01239648, 01239654, 01239660, 01241993, 01242001, 01242018, 01242024, 01248340, 01248357, 01260482, 01260499, 01260507, 01260542, 01260559, 01260565, 01263055, 01263061, 01277258, 01277264, 01277270, 01309596, 01417601, 02160564, 02160587, 02160601, 04130952, 05126585, 05126616, 05126651, 05958110, 05958127, 05958133, 06077469, 08540291, 08540322, 08540345, 08540368, 08540374, 09686163
ES	Centro de información online de medicamentos de la AEMPS	61910
FI	Lääkealan turvallisuus- ja kehittämiskeskus	004955, 011552, 075069, 085969, 086108, 171000
FR	Base de données publique des médicaments	63361640, 68712285
GB	Medicines & Healthcare Products Regulatory Agency	19949, 19963, 381694, 381696, 47227
HK	Department of Health Drug Office	44732, 44733, 60536
HR	Agencija za lijekove i medicinske proizvode	HR-H-099579965, HR-H-450430371
IE	Health Products Regulatory Authority	48222, 48233, 48246, 48284, 48287, 48288, 48294, 48296, 48297
IT	Agenzia del Farmaco	033303037, 033303049, 033303330, 033303417
MT	Medicines Authority	MA1470/00701, MA1470/01001, MA1470/01002, PI1438/06101A, PI1438/06102A, PI908/06801A, PI908/06802A
NL	Z-Index G-Standaard, PRK	48747, 76937
NZ	Medicines and Medical Devices Safety Authority	13921, 14460, 14461, 7592, 7593, 8755, 8756
PL	Rejestru Produktów Leczniczych	100234048
SG	Health Sciences Authority	11699P, 11704P, 14199P
TN	Direction de la Pharmacie et du Médicament	5933071, 5933072
TR	İlaç ve Tıbbi Cihaz Kurumu	8699809090255, 8699809090262
ZA	Health Products Regulatory Authority	32/5.7.1/0446, 32/5.7.1/0447, 42/5.7.1/0339