FDA label

What is Adderall used for?

Adderall contains dextroamphetamine and amphetamine. The FDA-approved uses below are 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 for Adderall lists this use: Attention Deficit Hyperactivity Disorder (ADHD).

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Adderall, tablet

Indications and Usage, quoted from the label by Teva Pharmaceuticals USA, Inc. (ANDA040422). Cross-references to other label sections are left out.

Adderall® (Dextroamphetamine saccharate, amphetamine aspartate, dextroamphetamine sulfate and amphetamine sulfate tablets (Mixed salts of a single entity amphetamine product)) is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) and Narcolepsy.

Attention Deficit Hyperactivity Disorder (ADHD)

A diagnosis of Attention Deficit Hyperactivity Disorder (ADHD; DSM-IV®) implies the presence of hyperactive-impulsive or inattentive symptoms that caused impairment and were present before age 7 years. The symptoms must cause clinically significant impairment, e.g., in social, academic, or occupational functioning, and be present in two or more settings, e.g., school (or work) and at home. The symptoms must not be better accounted for by another mental disorder. For the Inattentive Type, at least six of the following symptoms must have persisted for at least 6 months: lack of attention to details/careless mistakes; lack of sustained attention; poor listener; failure to follow through on tasks; poor organization; avoids tasks requiring sustained mental effort; loses things; easily distracted; forgetful. For the Hyperactive-Impulsive Type, at least six of the following symptoms must have persisted for at least 6 months: fidgeting/squirming; leaving seat; inappropriate running/climbing; difficulty with quiet activities; “on the go;” excessive talking; blurting answers; can't wait turn; intrusive. The Combined Type requires both inattentive and hyperactive-impulsive criteria to be met.

Source: DailyMed label, set id f22635fe-821d-4cde-aa12-419f8b53db81, version 21, effective May 29, 2024. NDC 57844-105, one of 7 listings for this product.

Adderall, capsule, extended release

Indications and Usage, quoted from the label by Takeda Pharmaceuticals America, Inc. (NDA021303). Cross-references to other label sections are left out.

Attention Deficit Hyperactivity Disorder

ADDERALL XR is indicated for the treatment of Attention Deficit Hyperactivity Disorder (ADHD) in adults and pediatric patients 6 years and older.

Limitations of Use The use of ADDERALL XR is not recommended in pediatric patients younger than 6 years of age because they had higher plasma exposure and a higher incidence of adverse reactions (e.g., weight loss) than patients 6 years and older at the same dosage.

Source: DailyMed label, set id aff45863-ffe1-4d4f-8acf-c7081512a6c0, version 38, effective April 30, 2026. NDC 54092-381, one of 6 listings for this product.

Questions

What is Adderall used for?

The FDA label for Adderall lists this use: Attention Deficit Hyperactivity Disorder (ADHD).

What drug class is Adderall?

FDA lists dextroamphetamine and amphetamine in the Central Nervous System Stimulant 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.

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