Regulatory PathRegulatory requirements compared

Active substance

Tafluprost

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
Novanza0.015 mg/mlEye drops, solution in single-dose container · Ophthalmic use30 Single Dose ContainerSAR 56.55Generic · PrescriptionJamjoom Pharmaceuticals Factory CompanyValid
SAFLUTAN 15MCG/ML EYE DROPS15 µgEye drops, solution in single-dose container · Ophthalmic use30 Single Dose ContainerSAR 60.60NCE · PrescriptionMUNDIPHARMA PTY LTDValid
Indications — CHI Daman Drug Formulary

OPEN ANGLE GLUCOMA

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

ProductStrengthForm · routeApplicantStatusFirst approved
ZIOPTAN0.0015%solution/drops · ophthalmicTHEA PHARMAPrescription10 Feb 2012
TAFLUPROST0.0015%solution/drops · ophthalmicMICRO LABSPrescription19 Aug 2019
TAFLUPROST0.0015%solution/drops · ophthalmicSANDOZPrescription28 Jan 2022
TAFLUPROST0.0015%solution/drops · ophthalmicINGENUS PHARMS LLCPrescription5 Apr 2024

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
US NADACTAFLUPROST 0.0015% EYE DROP$2.4535per EA23 Sep 2026
US NADACZIOPTAN 0.0015% EYE DROP$8.48561per EA23 Sep 2026
NHS Drug TariffTafluprost 15micrograms/ml eye drops£11.393 ml1 Oct 2026
NHS Drug TariffTafluprost 15micrograms/ml eye drops 0.3ml unit dose preservative free£12.2030 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

  • US FDA 25 Feb 2026 ZIOPTAN — safety-related labeling change
    Labeling sections changed: Warnings and Precautions; Use in Specific Populations; Patient Counseling Information / Patient Information / Medication Guide

All safety entries for tafluprost →

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.