Regulatory PathRegulatory requirements compared

Active substance

Eprosartan

Open in the medicines table

SFDA Saudi Arabia — SFDA human drug list

Trade nameStrengthForm · routePackPublic priceTypeCompanyStatus
TEVETEN 600MG TAB600 mgFilm-coated tablet · Oral use28 BlisterSAR 76.50NCE · PrescriptionABBOTT BIOLOGICALSValid
Indications — CHI Daman Drug Formulary

CHRONIC KIDNEY DISEASE; CORONARY ARTERY DISEASE; HYPERTENSION; SICKLE CELL DISEASE - ALBUMINURIA MANAGEMENT; SYSTEMIC LUPUS ERYTHEMATOSUS

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

ProductStrengthForm · routeApplicantStatusFirst approved
TEVETENEQ 300MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 400MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**; EQ 600MG BASE **Federal Register determination that product was not discontinued or withdrawn for safety or effectiveness reasons**tablet · oralABBVIEDiscontinued22 Dec 1997
EPROSARTAN MESYLATEEQ 400MG BASE; EQ 600MG BASEtablet · oralPHARMOBEDIENTDiscontinued16 Nov 2011

Prices — United States and England

SourceProduct as listedPriceUnit / packDate
NHS Drug TariffEprosartan 400mg tablets£26.5756 tablet1 Oct 2026
NHS Drug TariffEprosartan 600mg tablets£17.2628 tablet1 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.

Combinations containing Eprosartan

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.