TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ONTRALFY

TIZANIDINE HYDROCHLORIDE
Approved 2024-12-12
1
Indication
--
Phase 3 Trials
1
Years on Market

Details

Status
Prescription
First Approved
2024-12-12
Routes
ORAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: TIZANIDINE HYDROCHLORIDE

ONTRALFY Approval History

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What ONTRALFY Treats

1 indications

ONTRALFY is approved for 1 conditions since its original approval in 2024. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Spasticity
Source: FDA Label
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Active Pipeline

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Ongoing clinical trials by development phase

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Key Completed Trials

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Completed studies with published results, ranked by significance

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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.

ONTRALFY FDA Label Details

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Indications & Usage

FDA Label (PDF)

Ontralfy is indicated for the treatment of spasticity in adults. Ontralfy is a central alpha-2-adrenergic agonist indicated for the treatment of spasticity in adults.

ONTRALFY Patents & Exclusivity

Latest Patent: May 2042

Patents (2 active)

US12263158 Expires May 7, 2042
US12042484 Expires May 7, 2042
Source: FDA Orange Book

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Data Sources

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