DUOTRAV

This brand name is authorized in Australia, Austria, Canada, Croatia, Cyprus, Ecuador, Estonia, Finland, France, Germany, Hong Kong SAR China, Ireland, Israel, Italy, Japan, Lithuania, Netherlands, New Zealand, Nigeria, Poland, Romania, Singapore, South Africa, Spain, Tunisia, Turkey, UK.

Active ingredients

The drug DUOTRAV contains a combination of these active pharmaceutical ingredients (APIs):

1	Travoprost UNII WJ68R08KX9 - TRAVOPROST
	Travoprost, a prostaglandin F2α analogue, is a highly selective full agonist which has a high affinity for the prostaglandin FP receptor, and reduces the intraocular pressure by increasing the outflow of aqueous humour via trabecular meshwork and uveoscleral pathways.
	Read more about Travoprost
2	Timolol UNII P8Y54F701R - TIMOLOL MALEATE
	Timolol is a non-selective beta-adrenergic receptor blocking agent that does not have significant intrinsic sympathomimetic, direct myocardial depressant, or local anaesthetic activity. Timolol reduces intra-ocular pressure, whether or not this is associated with glaucoma.
	Read more about Timolol

Medicine classification

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

ATC Group		Classification
S01ED51	Timolol, combinations	S Sensory organs → S01 Ophthalmologicals → S01E Antiglaucoma preparations and miotics → S01ED Beta blocking agents
Discover more medicines within S01ED51

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	5555J, 9057Q
CA	Health Products and Food Branch	02278251
DE	Bundesinstitut für Arzneimittel und Medizinprodukte	00890494, 00890502, 16700900, 16930907, 17483190
EC	Agencia Nacional de Regulación, Control y Vigilancia Sanitaria	367470813
EE	Ravimiamet	1243763, 1243774, 1243785
ES	Centro de información online de medicamentos de la AEMPS	06338001
FI	Lääkealan turvallisuus- ja kehittämiskeskus	124870, 573177
FR	Base de données publique des médicaments	63633802
GB	Medicines & Healthcare Products Regulatory Agency	103205, 103206, 175383, 182540, 201631, 375915, 376320
HK	Department of Health Drug Office	55178
IE	Health Products Regulatory Authority	22511, 22539, 22560, 22571
IL	מִשְׂרַד הַבְּרִיאוּת	6407
IT	Agenzia del Farmaco	037104015
JP	医薬品医療機器総合機構	1319820Q1022
LT	Valstybinė vaistų kontrolės tarnyba	1005140, 1027899, 1027900, 1079985, 1079986, 1079987
NG	Registered Drug Product Database	A4-3210
Switch country to Nigeria in order to find specific presentations of DUOTRAV
NL	Z-Index G-Standaard, PRK	80888
NZ	Medicines and Medical Devices Safety Authority	11741
PL	Rejestru Produktów Leczniczych	100160611
RO	Agenția Națională a Medicamentului și a Dispozitivelor Medicale	W64597001
SG	Health Sciences Authority	13722P
TN	Direction de la Pharmacie et du Médicament	1903061, 20833041
TR	İlaç ve Tıbbi Cihaz Kurumu	8699504612042
ZA	Health Products Regulatory Authority	A40/15.4/0511