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YUPELRI

LAMA NEB

Revefenacin · Viatris Specialty LLC (with Theravance Biopharma)

Clinical Reference · Data reviewed June 2026

Active Medication & Mechanism

  • Revefenacin LAMA
    175 mcg per 3 mL unit-dose vial

    Long-acting muscarinic antagonist (anticholinergic). Inhibits the M3 receptor on airway smooth muscle, producing sustained bronchodilation with once-daily dosing.

FDA-Approved Dosing — Strength × Indication

175 mcg/3 mL 1 vial (175 mcg) nebulized once daily → 175 mcg
COPD FDA Approved
Maintenance treatment of COPD in adults. Administer via a standard jet nebulizer with a mouthpiece connected to an air compressor (studied with the PARI LC Sprint nebulizer and PARI Trek S compressor).
Asthma Not Approved
Yupelri is not indicated for asthma.

All regimens shown apply to adults (≥18 years) unless otherwise noted · verify against current labelling

Not a rescue inhaler. Not for acute bronchospasm or rescue. Use a SABA.

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For educational reference by healthcare professionals. Not medical advice and not for use in clinical decision-making. This workspace is not a substitute for clinical judgement, prescribing information, or product monographs — always verify doses and indications against the most current labelling. If you are a patient, do not use this site to make medication decisions — speak with your clinician.

Device images are original illustrations for identification aid only — actual devices and packaging may differ. This site is not affiliated with or endorsed by any pharmaceutical manufacturer. Clinical data last reviewed: June 2026.

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