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Ocupress (CARTEOLOL)

Novartis · FDA-approved approved Small molecule Quality 60/100

Ocupress (Carteolol) is a beta-adrenergic blocker, a small molecule drug developed by Novartis. It targets the beta-1 adrenergic receptor to treat hypertensive disorders, ocular hypertension, and open-angle glaucoma. Originally approved by the FDA in 1988, Ocupress is now off-patent with multiple generic manufacturers. Its half-life is approximately 4.7 hours, and it has a bioavailability of 88%. As a beta-blocker, Ocupress is used to reduce intraocular pressure and treat glaucoma.

At a glance

Generic nameCARTEOLOL
SponsorNovartis
Drug classbeta-Adrenergic Blocker
TargetBeta-1 adrenergic receptor
ModalitySmall molecule
Therapeutic areaCardiovascular
PhaseFDA-approved
First approval1988

Approved indications

Common side effects

Drug interactions

Key clinical trials

Primary sources

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SourceUsed for
FDA labelMechanism, indications, dosing, boxed warnings, drug interactions
ClinicalTrials.govTrial enrolment, design, endpoints, results

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