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Two medicines, side by side

Dexmethylphenidate vs lisdexamfetamine

Dexmethylphenidate and lisdexamfetamine are both labeled for ADHD. Drugs@FDA records approvals of dexmethylphenidate since 2001 and of lisdexamfetamine since 2007. Pharmacies paid $1.45 per dexmethylphenidate ER 10 mg capsule and $2.44 per lisdexamfetamine 20 mg capsule (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. How each works, in its label's words: Dexmethylphenidate, “Dexmethylphenidate hydrochloride is a CNS stimulant.”; Lisdexamfetamine, “Lisdexamfetamine is a prodrug of dextroamphetamine.”

Check it at the source: the dexmethylphenidate FDA label on DailyMed (effective May 30, 2024); the lisdexamfetamine FDA label on DailyMed (effective April 30, 2026).

Highlights of the dexmethylphenidate record

Dexmethylphenidate (Focalin) · label of May 30, 2024

Boxed warning

ABUSE, MISUSE, AND ADDICTION Focalin has 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 Focalin, 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 Focalin, assess each patient’s risk for abuse, misuse, and addiction.

Used for

From the label: indications

Focalin is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) [see Clinical Studies ( 14 )]. Focalin is a central nervous system (CNS) stimulant indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) ( 1 ).

On the market

Earliest approval on file
November 13, 2001
Generic labelers
13 labelers
Pharmacy cost
$1.45 per capsule

Supply and safety

Shortage
No current entry
Recalls
2

Highlights of the lisdexamfetamine record

Lisdexamfetamine (Vyvanse) · label of April 30, 2026

Boxed warning

ABUSE, MISUSE, AND ADDICTION VYVANSE has 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 VYVANSE, 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 VYVANSE, assess each patient's risk for abuse, misuse, and addiction.

Used for

From the label: indications

VYVANSE ® is indicated for the treatment of: Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older [see Clinical Studies (14.1) ]. Moderate to severe binge eating disorder (BED) in adults [see Clinical Studies (14.2) ]. […]

On the market

Earliest approval on file
February 23, 2007
Generic labelers
19 labelers
Pharmacy cost
$2.44 per capsule

Supply and safety

Shortage
In shortage
Recalls
11

Source: FDA drug labels via openFDA (Dexmethylphenidate label of May 30, 2024, Lisdexamfetamine label of April 30, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do dexmethylphenidate and lisdexamfetamine differ on the record?

How each works, in its label's words: Dexmethylphenidate, “Dexmethylphenidate hydrochloride is a CNS stimulant.”; Lisdexamfetamine, “Lisdexamfetamine is a prodrug of dextroamphetamine.”

Both are in FDA's class central nervous system stimulants.

Half-life, in each label's words: Dexmethylphenidate, “The mean terminal elimination half-life of dexmethylphenidate was approximately 2.2 hours.”; Lisdexamfetamine, “The plasma elimination half-life of dextroamphetamine was approximately 8.6 to 9.5 hours in pediatric patients 6 to 12 …”

Both labels carry a boxed warning; the records quote them.

Generics: dexmethylphenidate since 2007; lisdexamfetamine since 2023 (Drugs@FDA).

DexmethylphenidateLisdexamfetamine
Labeled forADHDADHD, Binge eating disorder
Pharmacologic classCentral Nervous System StimulantCentral Nervous System Stimulant
How it works (label)Dexmethylphenidate hydrochloride is a CNS stimulant. The mode of therapeutic action in ADHD is not known.Lisdexamfetamine is a prodrug of dextroamphetamine. Amphetamines are non-catecholamine sympathomimetic amines with CNS stimulant activity. The exact mode of therapeutic action in ADHD and BED is not known.
Half-life (label)The mean terminal elimination half-life of dexmethylphenidate was approximately 2.2 hours.The plasma elimination half-life of dextroamphetamine was approximately 8.6 to 9.5 hours in pediatric patients 6 to 12 years and 10 to 11.3 hours in healthy adults.
Earliest approval on file (Drugs@FDA)November 13, 2001February 23, 2007
First generic approvedJanuary 29, 2007August 25, 2023
Generic labelers (NDC)13 labelers19 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$1.45 per capsule (Dexmethylphenidate ER 10 mg capsule)$2.44 per capsule (Lisdexamfetamine 20 mg capsule)
12-month price change+4%-32%
Boxed warningYesYes
Shortage nowNo current entryIn shortage
Recalls recorded211
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)4,20734,602
DEA scheduleCIICII

Source: Drugs@FDA, FDA NDC Directory, CMS NADAC of October 7, 2026, FDA shortages and recalls, FAERS via openFDA (FDA files October 8, 2026)

What do the labels say about using others of their kind?

Lisdexamfetamine label, warnings and precautions

If concomitant use of VYVANSE with other serotonergic drugs or CYP2D6 inhibitors is clinically warranted, initiate VYVANSE with lower doses, monitor patients for the emergence of serotonin syndrome during drug initiation or titration, and inform patients of the increased risk for serotonin syndrome.

Source: FDA drug labels via openFDA

What next?

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