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Two medicines, side by side

Guanfacine vs methylphenidate

Guanfacine and methylphenidate are both labeled for ADHD. Drugs@FDA records approvals of guanfacine since 1986 and of methylphenidate since 1955. Pharmacies paid $0.147 per guanfacine 1 mg tablet and $0.158 per methylphenidate 10 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Methylphenidate's other strengths are brand-only: $2.43 per mL (Quillivant XR 25 mg/5 mL suspension). In FDA's classes, guanfacine is a central alpha-2 adrenergic agonist and methylphenidate a central nervous system stimulant.

Check it at the source: the guanfacine FDA label on DailyMed (effective June 23, 2025); the methylphenidate FDA label on DailyMed (effective July 31, 2026).

Highlights of the guanfacine record

Guanfacine (Intuniv) · label of June 23, 2025

Used for

From the label: indications

INTUNIV ® is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) as monotherapy and as adjunctive therapy to stimulant medications [see Clinical Studies (14) ]. INTUNIV is a central alpha 2A -adrenergic receptor agonist indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) as monotherapy and as adjunctive therapy to stimulant medications ( 1 , 14 ).

On the market

Earliest approval on file
October 27, 1986
Generic labelers
36 labelers
Pharmacy cost
$0.147 per tablet

Supply and safety

Shortage
A presentation being discontinued
Recalls
1

Highlights of the methylphenidate record

Methylphenidate (Ritalin) · label of July 31, 2026

Boxed warning

ABUSE, MISUSE, AND ADDICTION Methylphenidate HCl Extended-Release Capsules CD 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 Methylphenidate HCl Extended-Release Capsules CD, 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.

Used for

From the label: indications

Methylphenidate HCl Extended-Release Capsules CD is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in pediatric patients 6 to 15 years of age. […]

On the market

Earliest approval on file
December 5, 1955
Generic labelers
31 labelers
Pharmacy cost
$0.158 per tablet

Supply and safety

Shortage
In shortage
Recalls
55

Source: FDA drug labels via openFDA (Guanfacine label of June 23, 2025, Methylphenidate label of July 31, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do guanfacine and methylphenidate differ on the record?

In FDA's classes, guanfacine is a central alpha-2 adrenergic agonist and methylphenidate a central nervous system stimulant.

How each works, in its label's words: Guanfacine, “Guanfacine is a central alpha 2A -adrenergic receptor agonist.”; Methylphenidate, “Methylphenidate hydrochloride is a central nervous system (CNS) stimulant.”

Only the methylphenidate label carries a boxed warning.

Generics: guanfacine since 1995; methylphenidate since 1977 (Drugs@FDA).

DEA schedule: guanfacine none; methylphenidate CII.

GuanfacineMethylphenidate
Labeled forADHD, High blood pressureADHD
Pharmacologic classCentral alpha-2 Adrenergic AgonistCentral Nervous System Stimulant
How it works (label)Guanfacine is a central alpha 2A -adrenergic receptor agonist. Guanfacine is not a central nervous system (CNS) stimulant. The mechanism of action of guanfacine in ADHD is not known.Methylphenidate hydrochloride is a central nervous system (CNS) stimulant. The mode of therapeutic action in ADHD is not known.
Half-life (label)n/an/a
Earliest approval on file (Drugs@FDA)October 27, 1986December 5, 1955
First generic approvedOctober 17, 1995December 23, 1977
Generic labelers (NDC)36 labelers31 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.147 per tablet (Guanfacine 1 mg tablet)$0.158 per tablet (Methylphenidate 10 mg tablet)
12-month price change-5%-14%
Boxed warningNoYes
Shortage nowA presentation being discontinuedIn shortage
Recalls recorded155
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)7,82573,102
DEA schedulenoneCII

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

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