Saturday, July 11, 2026

Drug profile · INN

timolol maleate

timolol maleate (TIMOPTIC IN OCUDOSE) is a beta-1 adrenergic receptor antagonist. Associated with Amneal Pharma Europe Ltd. Route of administration: ophthalmic. Current US regulatory status: approved.

FDA: approved
US status approved
Patents linked 0
Pipeline programs 0
News articles 0
Drug details — timolol maleate
US status
approved
Class
Route
OPHTHALMIC
Patents
0
Programs
0
Data quality
0.89

Quick answer

timolol maleate (TIMOPTIC IN OCUDOSE) is a beta-1 adrenergic receptor antagonist. Associated with Amneal Pharma Europe Ltd. Route of administration: ophthalmic. Current US regulatory status: approved.

Key facts

INN timolol maleate
Brand TIMOPTIC IN OCUDOSE
Mechanism Beta-1 adrenergic receptor antagonist
Target Beta-1 adrenergic receptor
Route OPHTHALMIC
Formulation SOLUTION, GEL FORMING/DROPS

Mechanism of action

Beta-1 adrenergic receptor antagonist

Primary target: Beta-1 adrenergic receptor

Approval history

Authority Status Date
FDA approved

Related & competitor drugs

  1. acebutolol hydrochloride Beta-1 adrenergic receptor antagonist
  2. atenolol Beta-1 adrenergic receptor antagonist
  3. bisoprolol fumarate Beta-1 adrenergic receptor antagonist
  4. dobutamine hydrochloride Beta-1 adrenergic receptor agonist
  5. dopamine hydrochloride Cardiovascular system (C01)
  6. esmolol hydrochloride Beta-2 adrenergic receptor antagonist

Frequently asked questions

What is timolol maleate?

timolol maleate (TIMOPTIC IN OCUDOSE) is a beta-1 adrenergic receptor antagonist. Associated with Amneal Pharma Europe Ltd. Route of administration: ophthalmic. Current US regulatory status: approved.

What is the brand name for timolol maleate?

TIMOPTIC IN OCUDOSE is a marketed brand name for timolol maleate. Check FDA Drugs@FDA for the current US label holder and prescribing information.

What is the US approval status of timolol maleate?

timolol maleate has approved status in the United States according to our Drugs@FDA-derived records. Verify on the official FDA label before clinical or commercial decisions.