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Two medicines, side by side

Atomoxetine vs clonidine

Atomoxetine and clonidine are both labeled for ADHD. Drugs@FDA records approvals of atomoxetine since 2002 and of clonidine since 1974. Pharmacies paid $0.442 per atomoxetine HCl 40 mg capsule and $0.0241 per clonidine HCl 0.1 mg tablet (NADAC, October 7, 2026); the strengths differ, so the two prices are not like for like. Clonidine's other strengths are brand-only: $1.53 per mL (Javadin 0.02 mg/mL solution). In FDA's classes, atomoxetine is a norepinephrine reuptake inhibitor and clonidine a central alpha-2 adrenergic agonist.

Check it at the source: the atomoxetine FDA label on DailyMed (effective May 25, 2026); the clonidine FDA label on DailyMed (effective March 30, 2026).

Highlights of the atomoxetine record

Atomoxetine (Strattera) · label of May 25, 2026

Boxed warning

SUICIDAL IDEATION IN CHILDREN AND ADOLESCENTS Atomoxetine increased the risk of suicidal ideation in short-term studies in children or adolescents with Attention-Deficit/Hyperactivity Disorder (ADHD). Anyone considering the use of atomoxetine in a child or adolescent must balance this risk with the clinical need. Co-morbidities occurring with ADHD may be associated with an increase in the risk of suicidal ideation and/or behavior.

Used for

From the label: indications

Atomoxetine capsule is a selective norepinephrine reuptake inhibitor indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD). ( 1.1 ) 1.1 Attention-Deficit/Hyperactivity Disorder (ADHD) Atomoxetine capsule is indicated for the treatment of Attention-Deficit/Hyperactivity Disorder (ADHD). […]

On the market

Earliest approval on file
November 26, 2002
Generic labelers
20 labelers
Pharmacy cost
$0.442 per capsule

Supply and safety

Shortage
No current entry
Recalls
15

Highlights of the clonidine record

Clonidine (Catapres) · label of March 30, 2026

Used for

From the label: indications

Clonidine hydrochloride tablets are indicated in the treatment of hypertension. Clonidine hydrochloride tablets may be employed alone or concomitantly with other antihypertensive agents.

On the market

Earliest approval on file
September 3, 1974
Generic labelers
43 labelers
Pharmacy cost
$0.0241 per tablet

Supply and safety

Shortage
No current entry
Recalls
16

Source: FDA drug labels via openFDA (Atomoxetine label of May 25, 2026, Clonidine label of March 30, 2026); NDC Directory, Drugs@FDA, NADAC, FDA shortages and recalls (October 8, 2026)

How do atomoxetine and clonidine differ on the record?

In FDA's classes, atomoxetine is a norepinephrine reuptake inhibitor and clonidine a central alpha-2 adrenergic agonist.

Half-life, in each label's words: Atomoxetine, “Atomoxetine has a half-life of about 5 hours.”; Clonidine, “Following intravenous administration, clonidine displays biphasic disposition with a distribution half-life of about 20 …”

Only the atomoxetine label carries a boxed warning.

Generics: atomoxetine since 2010; clonidine since 1986 (Drugs@FDA).

AtomoxetineClonidine
Labeled forADHDHigh blood pressure, ADHD, Pain
Pharmacologic classNorepinephrine Reuptake InhibitorCentral alpha-2 Adrenergic Agonist
How it works (label)The precise mechanism by which atomoxetine produces its therapeutic effects in Attention-Deficit/Hyperactivity Disorder (ADHD) is unknown, but is thought to be related to selective inhibition of the pre-synaptic norepinephrine transporter …n/a
Half-life (label)Atomoxetine has a half-life of about 5 hours.Following intravenous administration, clonidine displays biphasic disposition with a distribution half-life of about 20 minutes and an elimination half-life ranging from 12 to 16 hours.
Earliest approval on file (Drugs@FDA)November 26, 2002September 3, 1974
First generic approvedSeptember 16, 2010July 1, 1986
Generic labelers (NDC)20 labelers43 labelers
Pharmacy cost (NADAC, each one's most listed form; strengths differ)$0.442 per capsule (Atomoxetine HCl 40 mg capsule)$0.0241 per tablet (Clonidine HCl 0.1 mg tablet)
12-month price change-27%-3%
Boxed warningYesNo
Shortage nowNo current entryNo current entry
Recalls recorded1516
FAERS reports (a report is not proof of cause; counts follow how widely a medicine is used)26,96957,116
DEA schedulenonenone

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 next?

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