TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

EVEKEO ODT

AMPHETAMINE SULFATE
Approved 2019-01-30
2
Indications
--
Phase 3 Trials
7
Years on Market

Details

Status
Discontinued
First Approved
2019-01-30
Routes
ORAL
Dosage Forms
TABLET, ORALLY DISINTEGRATING

Companies

Active Ingredient: AMPHETAMINE SULFATE

EVEKEO ODT Approval History

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What EVEKEO ODT Treats

2 FDA approvals

Originally approved for its first indication in 2019 . Covers 2 distinct patient populations.

  • Other (2)
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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.

EVEKEO ODT FDA Label Details

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EVEKEO ODT Patents & Exclusivity

Latest Patent: Mar 2037

Patents (70 active)

US11896562 Expires Mar 10, 2037
US10441554 Expires Mar 10, 2037
US11160772 Expires Mar 10, 2037
+ 60 more patents
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.