TheraRadar
Data updated: May 26, 2026

JORNAY PM (methylphenidate hydrochloride)

CNS Approved 2018-08-08

Jornay PM is a central nervous system stimulant used for children between the ages of 6 and 12. It treats Attention Deficit Hyperactivity Disorder (ADHD) in this pediatric population. This medication helps patients with ADHD manage their symptoms.

Source: FDA Label • IRONSHORE PHARMS

How JORNAY PM Works

This medication works by acting as a central nervous system stimulant. While it is used to manage ADHD, the specific way it functions to produce a therapeutic effect is not known.

1
Indication
--
Phase 3 Trials
7
Years on Market

Details

Status
Prescription
First Approved
2018-08-08
Patent Cliff
2032

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Routes
ORAL
Dosage Forms
CAPSULE, EXTENDED RELEASE

Companies

Active Ingredient: METHYLPHENIDATE HYDROCHLORIDE

JORNAY PM Approval History

2019
2020
2021
2022
2023
2024
2025
2026
Original
New Indication
New Form
Label Update
25 FDA actions from 2018 to 2025
Sep 2025 SUPPL
Label · Labeling
Oct 2023 SUPPL
Label · Labeling
Jun 2021 SUPPL
Label · Labeling

What JORNAY PM Treats

1 indications

JORNAY PM is approved for 1 conditions since its original approval in 2018. These indications span multiple therapeutic areas including oncology, immunology, and more.

  • Attention Deficit Hyperactivity Disorder
Source: FDA Label

JORNAY PM Boxed Warning

ABUSE AND DEPENDENCE C N S stimulants, including methylphenidate hydrochloride extended-release capsules , other methylphenidate-containing products, and amphetamines, have a high potential for abuse and dependence. Assess the risk of abuse prior to prescribing, and monitor for signs of abuse and dependence while on therapy [see Warnings and Precautions ( 5.1 ), Drug Abuse and Dependence ( 9.2 , 9.3 )] . WARNING: ABUSE AND DEPENDENCE See full prescribing information for complete boxed warning. C...

JORNAY PM Competitive Set

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Filters applied: drops same-active-ingredient (505(b)(2) reformulations), route-mismatch (topical vs systemic), and cross-therapeutic-area matches in same-indication rings.

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Clinical Trial Registry

14 trials
Trial Sponsor ID Phase Status Title
NCT01628029 results posted 2012-0120 NCI-2012-01352, 2012-0120 Ph 2 active not recruiting Cognitive Behavioral Therapy and Multimodal Therapy in Treating Sleep Disturbance in Patients With Cancer
NCT05185583 77169 Ph 2 completed Methylphenidate in Childhood Apraxia of Speech
NCT06465641 KBGS_N_of_1 113883 Ph 4 recruiting Methylphenidate in KBG Syndrome: N-of-1 Series
NCT04152629 reFOQus CAN-MA-FOQ-001 Ph 4 completed Real World Evidence of the Efficacy and Safety of FOQUEST
NCT00763971 results posted SPD489-325 2008-000679-90 Ph 3 completed Randomized, Double-blind Safety and Efficacy Study of Lisdexamfetamine Dimesylate (LDX) in Children and Adolescents Aged 6-17
NCT01552902 results posted SPD489-406 2011-005452-34 Ph 4 completed Effectiveness of Vyvanse Compared to Concerta in Adolescents With Attention-deficit/Hyperactivity Disorder
NCT01183234 results posted SPD544-101 Ph 1 completed SPD544 High Strength Bioequivalence Study
NCT01552915 results posted SPD489-405 Ph 4 completed Effectiveness of Vyvanse Compared to Concerta in Adolescents With Attention-deficit/Hyperactivity Disorder
NCT02247986 140193 14-M-0193 Ph 1, Ph 2 withdrawn Investigating the Impact of Methylphenidate on Neural Response in Disruptive Behavioral Disorder
NCT01914822 275-13-RMB Ritalin version 5 Ph 2 completed The Effect Methylphenidate Hydrochloride on Pain and Auditory Sensitivity in Healthy Subjects
NCT00376675 results posted NCCTG-N05C7 NCI-2012-02701, CDR0000495148 Ph 3 completed Methylphenidate in Treating Patients With Fatigue Caused by Cancer
NCT00593853 LEUPR_L_01 07-0350-C Ph 2 terminated Efficacy Study of Methylphenidate Hydrochloride to Reduce Fatigue in Prostate Cancer Patients Receiving Hormone Therapy
NCT01348607 results posted SCUSF 0803 SCUSF-0803, 5U10CA081920-11 Ph 2 terminated Methylphenidate HCl or Modafinil in Treating Young Patients With Excessive Daytime Sleepiness After Cancer Therapy
NCT00730249 QUMEA 6520-0650-13 Ph 3 completed Quality Assurance of Administering Methylphenidate in Adults With Attention Deficit Hyperactivity Disorder (ADHD) - QUMEA
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Active Pipeline

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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.

JORNAY PM FDA Label Details

Indications & Usage

FDA Label (PDF)

JORNAY PM is indicated for the treatment of Attention Deficit Hyperactivity Disorder.

⚠️ BOXED WARNING

WARNING: ABUSE AND DEPENDENCE C N S stimulants, including methylphenidate hydrochloride extended-release capsules , other methylphenidate-containing products, and amphetamines, have a high potential for abuse and dependence. Assess the risk of abuse prior to prescribing, and monitor for signs of abu...

View full patent landscape →
16 OB patents · 9 families · 87 international docs across 15 countries

JORNAY PM Patents & Exclusivity

Latest Patent: Mar 2032

Patents (16 active)

US9028868 Expires Mar 23, 2032
US9034902 Expires Mar 23, 2032
US8916588 Expires Mar 23, 2032
US9603809 Expires Mar 23, 2032
US10292937 Expires Mar 23, 2032
US10617651 Expires Mar 23, 2032
US10881618 Expires Mar 23, 2032
US11911518 Expires Mar 23, 2032
US11241391 Expires Mar 23, 2032
US11241392 Expires Mar 23, 2032
US10182995 Expires Mar 23, 2032
US8927010 Expires Mar 23, 2032
US9023389 Expires Mar 23, 2032
US10905652 Expires Mar 23, 2032
US9498447 Expires Mar 23, 2032
US9283214 Expires Mar 23, 2032
Source: FDA Orange Book

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Revenue Insights

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Patent Timeline

  • Cliff: 2032
  • 400 active patents

Trial Analysis

  • Clinical trial tracking
  • Development stage analysis

Competitive Landscape

  • 20 similar drugs
  • Same target/indication analysis
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Data Sources

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