Regulatory PathRegulatory requirements compared

Active substance

Travoprost

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
Ravopro0.04 mg/mlEye drops · Ocular use1 Dropper ContainerSAR 43.05Generic · PrescriptionAdvanced Pharmaceutical IndustriesValid
TRAVATAN EYE DROP0.004 µ/mlEye drops · Ocular use1 Dropper ContainerSAR 46.30Generic · PrescriptionNOVARTIS PHARMA AGValid
Indications — CHI Daman Drug Formulary

OPEN ANGLE GLUCOMA

US FDA United States — FDA approvals (Drugs@FDA)

ProductStrengthForm · routeApplicantStatusFirst approved
TRAVATAN Z0.004%solution/drops · ophthalmicSANDOZPrescription21 Sep 2006
TRAVOPROST0.004%solution/drops · ophthalmicCHARTWELL RXPrescription1 Mar 2013
TRAVOPROST0.004%solution/drops · ophthalmicAPOTEXPrescription10 Jul 2015
TRAVOPROST0.004%solution/drops · ophthalmicMYLANPrescription7 Jul 2017
TRAVOPROST0.004%solution/drops · ophthalmicMICRO LABSPrescription19 Mar 2021
IDOSE TR75MCGimplant · intracameralGLAUKOSPrescription13 Dec 2023
TRAVOPROST0.004%solution/drops · ophthalmicGLANDPrescription12 Jul 2024
TRAVOPROST0.004%solution/drops · ophthalmicSOMERSET THERAPS LLCPrescription23 Sep 2024
TRAVOPROST0.004%solution/drops · ophthalmicALEMBICPrescription17 Dec 2025
TRAVATAN0.004% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**solution/drops · ophthalmicALCON PHARMS LTDDiscontinued16 Mar 2001
IZBA0.003% **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**solution/drops · ophthalmicNOVARTISDiscontinued15 May 2014
TRAVOPROST0.004%solution/drops · ophthalmicALEMBICDiscontinued20 Dec 2019
TRAVOPROST0.004%solution/drops · ophthalmicLUPINDiscontinued3 May 2024

EMA European Union — centrally authorised medicines

Travatan Novartis Europharm Limited · Authorised · authorised 27 Nov 2001 · ATC S01EE04

Therapeutic indication (EMA)

Decrease of elevated intraocular pressure in adult patients with ocular hypertension or open-angle glaucoma (see section 5.1). Decrease of elevated intraocular pressure in paediatric patients aged 2 months to < 18 years with ocular hypertension or paediatric glaucoma (see section 5.1).

Izba Novartis Europharm Limited · Authorised · authorised 20 Feb 2014 · ATC S01EE04

Therapeutic indication (EMA)

Decrease of elevated intraocular pressure in adult patients with ocular hypertension or open-angle glaucoma (see section 5.1). Decrease of elevated intraocular pressure in paediatric patients aged 3 years to < 18 years with ocular hypertension or paediatric glaucoma.

Canada Canada — marketed products (Health Canada)

BrandDINStrengthForm · routeCompany
IZBA024579970.003 % / W/VSOLUTION · OPHTHALMICNOVARTIS PHARMACEUTICALS CANADA INC
JAMP TRAVOPROST Z025480890.004 % / W/VSOLUTION · OPHTHALMICJAMP PHARMA CORPORATION
SANDOZ TRAVOPROST024131670.004 % / W/VSOLUTION · OPHTHALMICSANDOZ CANADA INCORPORATED
TRAVATAN Z023180080.004 % / W/VSOLUTION · OPHTHALMICNOVARTIS PHARMACEUTICALS CANADA INC

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACTRAVATAN Z 0.004% EYE DROP$94.2313per ML23 Sep 2026
US NADACTRAVATAN Z 0.004% EYE DROP$94.29844per ML23 Sep 2026
US NADACTRAVOPROST 0.004% EYE DROP$8.39412per ML23 Sep 2026
US NADACTRAVOPROST 0.004% EYE DROP$9.74746per ML23 Sep 2026
NHS Drug TariffTravoprost 40micrograms/ml eye drops£2.292.5 ml1 Oct 2026
NHS Drug TariffTravoprost 40micrograms/ml eye drops 0.1ml unit dose preservative free£7.4930 unit dose1 Oct 2026

NADAC: average price US retail pharmacies pay to buy the medicine. NHS Drug Tariff Part VIIIA: basic price reimbursed to pharmacies in England and Wales.

Safety signals and safety-related labeling changes

All safety entries for travoprost →

Combinations containing Travoprost

Values as published by each source: SFDA human drug list (4-2026, as published by the Council of Health Insurance; indications from the CHI Daman Drug Formulary), Drugs@FDA, EMA medicines data, Health Canada Drug Product Database (Open Government Licence – Canada), CMS NADAC, NHS Drug Tariff Part VIIIA (NHSBSA Copyright, Open Government Licence v3.0), WHO Model List of Essential Medicines (CC BY 3.0 IGO; regrouped by active substance, not created by WHO), EMA PRAC, US FDA safety-related labeling changes and MHRA Drug Safety Update (Open Government Licence v3.0). Sources and reuse. Not a substitute for the official registers or the product information.