FDA label

What is Sunosi used for?

Sunosi contains solriamfetol. 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 says: “SUNOSI is indicated to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA).”

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Sunosi, tablet, film coated

Indications and Usage, quoted from the label by Axsome Therapeutics, Inc. (NDA211230). Cross-references to other label sections are left out.

SUNOSI is indicated to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA).

Limitations of Use

SUNOSI is not indicated to treat the underlying airway obstruction in OSA. Ensure that the underlying airway obstruction is treated (e.g., with continuous positive airway pressure (CPAP)) for at least one month prior to initiating SUNOSI for excessive daytime sleepiness. Modalities to treat the underlying airway obstruction should be continued during treatment with SUNOSI. SUNOSI is not a substitute for these modalities.

Source: DailyMed label, set id 362f206b-73e7-4009-8c34-5a9df55679ab, version 6, effective May 5, 2026. NDC 81968-350, one of 2 listings for this product.

Questions

What is Sunosi used for?

The FDA label says: “SUNOSI is indicated to improve wakefulness in adult patients with excessive daytime sleepiness associated with narcolepsy or obstructive sleep apnea (OSA).”

What drug class is Sunosi?

FDA lists solriamfetol in the Dopamine and 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.

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