FDA label
What is atomoxetine used for?
The FDA-approved uses of atomoxetine, quoted from the Indications and Usage section of its DailyMed label.
Source: DailyMed SPL label file dated 2026-10-23. Publisher page
The FDA label says: “Atomoxetine capsules are indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in adults and pediatric patients 6 years of age and older.”
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Atomoxetine, capsule
Indications and Usage, quoted from the label by Teva Pharmaceuticals USA, Inc. (ANDA079022). Cross-references to other label sections are left out.
Atomoxetine capsules are indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in adults and pediatric patients 6 years of age and older.
Atomoxetine capsules are indicated as an integral part of a total treatment program for ADHD that may include other measures (psychological, educational, social) for patients with ADHD.
Source: DailyMed label, set id 4953df7b-ccdb-452c-8699-5fd7259609b4, version 19, effective September 3, 2026. NDC 0093-3542, one of 128 listings for this product.
Questions
What is atomoxetine used for?
The FDA label says: “Atomoxetine capsules are indicated for the treatment of attention-deficit/hyperactivity disorder (ADHD) in adults and pediatric patients 6 years of age and older.”
What drug class is atomoxetine?
FDA lists atomoxetine in the Norepinephrine Reuptake Inhibitor established pharmacologic class.
Does this page cover off-label uses or dosing?
No. This page shows only the Indications and Usage section of the FDA label. Ask a pharmacist or prescriber about dosing.