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Data updated: Mar 10, 2026

BRIMONIDINE TARTRATE AND TIMOLOL MALEATE

BRIMONIDINE TARTRATE
Cardiovascular Approved 2022-04-04
10
Indications
--
Phase 3 Trials
3
Years on Market

Details

Status
Prescription
First Approved
2022-04-04
Routes
OPHTHALMIC
Dosage Forms
SOLUTION/DROPS

BRIMONIDINE TARTRATE AND TIMOLOL MALEATE Approval History

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What BRIMONIDINE TARTRATE AND TIMOLOL MALEATE Treats

2 indications

BRIMONIDINE TARTRATE AND TIMOLOL MALEATE is approved for 2 conditions since its original approval in 2022. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Glaucoma
  • Ocular Hypertension
Source: FDA Label

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Trial Timeline

Full development history with FDA approval milestones

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Understanding FDA Approval Types
Count Type What it means
- ORIG Original approval - drug first enters market
- SUPPL - Efficacy New indication (new disease/condition approved)
- SUPPL - Labeling Label text changes (warnings, dosing updates)
- SUPPL - Manufacturing Production changes (new facility)
- SUPPL - Chemistry Formulation changes (new dosage strength)

Green lines in the timeline show ORIG and Efficacy approvals - the clinically meaningful milestones.

BRIMONIDINE TARTRATE AND TIMOLOL MALEATE FDA Label Details

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Indications & Usage

Brimonidine tartrate and timolol maleate ophthalmic solution 0.2% /0.5% is an alpha-adrenergic receptor agonist with a beta-adrenergic receptor inhibitor indicated for the reduction of elevated intraocular pressure (IOP) in patients with glaucoma or ocular hypertension who require adjunctive or replacement therapy due to inadequately controlled IOP; the IOP-lowering of Brimonidine tartrate and timolol maleate ophthalmic solution dosed twice a day was slightly less than that seen with the concomitant administration of 0.5% timolol maleate ophthalmic solution dosed twice a day and 0.2% brimonidi...

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Data Sources

Data sourced from official FDA and NIH databases. Click links to verify on original sources.