TheraRadar

Pharma Intelligence, Simplified

Data updated: Mar 10, 2026

ARYNTA

LISDEXAMFETAMINE DIMESYLATE
Cardiovascular Approved 2025-06-16
1
Indication
--
Phase 3 Trials
0
Years on Market

Details

Status
Prescription
First Approved
2025-06-16
Routes
ORAL
Dosage Forms
SOLUTION

Companies

Active Ingredient: LISDEXAMFETAMINE DIMESYLATE

ARYNTA Approval History

Loading approval history...

What ARYNTA Treats

2 indications

ARYNTA is approved for 2 conditions since its original approval in 2025. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Attention Deficit Hyperactivity Disorder
  • Binge Eating Disorder
Source: FDA Label

ARYNTA Boxed Warning

ABUSE, MISUSE, AND ADDICTION Lisdexamfetamine dimesylate capsules have a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction. Misuse and abuse of CNS stimulants, including lisdexamfetamine dimesylate capsules, can result in overdose and death [see Overdosage (10) ] , and this risk is increased with higher doses or unapproved methods of administration, such as snorting or injection. Before prescribing lisdexamfetamine dimesylate ...

Drugs Similar to ARYNTA

FDA-approved drugs for similar conditions. Compare mechanisms and indications to understand treatment alternatives.

LISDEXAMFETAMINE DIMESYLATE
LISDEXAMFETAMINE DIMESYLATE
2 shared
LANNETT CO INC
Shared indications:
Attention Deficit Hyperactivity DisorderBinge Eating Disorder
VYVANSE
LISDEXAMFETAMINE DIMESYLATE
2 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity DisorderBinge Eating Disorder
ADDERALL XR 10
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADDERALL XR 15
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADDERALL XR 20
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADDERALL XR 25
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADDERALL XR 30
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADDERALL XR 5
AMPHETAMINE ASPARTATE
1 shared
Takeda
Shared indications:
Attention Deficit Hyperactivity Disorder
ADZENYS XR-ODT
AMPHETAMINE
1 shared
NEOS THERAPS
Shared indications:
Attention Deficit Hyperactivity Disorder
AMPHETAMINE SULFATE
AMPHETAMINE SULFATE
1 shared
PRINSTON INC
Shared indications:
Attention Deficit Hyperactivity Disorder
APTENSIO XR
METHYLPHENIDATE HYDROCHLORIDE
1 shared
RHODES PHARMS
Shared indications:
Attention Deficit Hyperactivity Disorder
AZSTARYS
DEXMETHYLPHENIDATE HYDROCHLORIDE
1 shared
COMMAVE THERAP
Shared indications:
Attention Deficit Hyperactivity Disorder
CONCERTA
METHYLPHENIDATE HYDROCHLORIDE
1 shared
Johnson & Johnson
Shared indications:
Attention Deficit Hyperactivity Disorder
COTEMPLA XR-ODT
METHYLPHENIDATE
1 shared
NEOS THERAPS INC
Shared indications:
Attention Deficit Hyperactivity Disorder
DAYTRANA
METHYLPHENIDATE
1 shared
NOVEN PHARMS INC
Shared indications:
Attention Deficit Hyperactivity Disorder
DEXEDRINE SPANSULE
DEXTROAMPHETAMINE SULFATE
1 shared
IMPAX LABS INC
Shared indications:
Attention Deficit Hyperactivity Disorder
DEXTROAMPHETAMINE SULFATE
DEXTROAMPHETAMINE SULFATE
1 shared
SPECGX LLC
Shared indications:
Attention Deficit Hyperactivity Disorder
DYANAVEL XR
AMPHETAMINE
1 shared
TRIS PHARMA INC
Shared indications:
Attention Deficit Hyperactivity Disorder
DYANAVEL XR 10
AMPHETAMINE
1 shared
TRIS PHARMA INC
Shared indications:
Attention Deficit Hyperactivity Disorder
DYANAVEL XR 15
AMPHETAMINE
1 shared
TRIS PHARMA INC
Shared indications:
Attention Deficit Hyperactivity Disorder
🔬

Active Pipeline

Pro

Ongoing clinical trials by development phase

Loading...

Key Completed Trials

Pro

Completed studies with published results, ranked by significance

Loading...
📊

Trial Timeline

Full development history with FDA approval milestones

Loading...
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.

ARYNTA FDA Label Details

Pro

Indications & Usage

FDA Label (PDF)

Lisdexamfetamine dimesylate capsules are indicated for the treatment of: Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older [see Clinical Studies ] Moderate to severe binge eating disorder (BED) in adults [see Clinical Studies ] . Lisdexamfetamine dimesylate capsules are a central nervous system (CNS) stimulant indicated for the treatment of : Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older Moderate to severe binge eating disorder (BED) in adults Limitations of Use : The use of lisdexamfetamine d...

⚠️ BOXED WARNING

WARNING: ABUSE, MISUSE, AND ADDICTION Lisdexamfetamine dimesylate capsules have a high potential for abuse and misuse, which can lead to the development of a substance use disorder, including addiction. Misuse and abuse of CNS stimulants, including lisdexamfetamine dimesylate capsules, can result in...

ARYNTA Patents & Exclusivity

Latest Patent: Aug 2040

Patents (2 active)

US11576878 Expires Aug 30, 2040
US12433859 Expires Apr 16, 2040
Source: FDA Orange Book

Want competitive intelligence?

See who's developing similar drugs and track their progress

View Pipeline Dashboard

Data Sources

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