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YUPELRI

Revefenacin

YUPELRI

LAMA NEB

Revefenacin · Viatris Specialty LLC (with Theravance Biopharma)

Clinical Reference

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 by Indication

// approval varies by strength + age
COPD
1/1 approved regimens
  • 175 mcg/3 mL FDA Approved
    Pop · Adults (≥18 years)
    1 vial (175 mcg) nebulized once daily
    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).
    Total · 175 mcg
Asthma
0/1 approved regimens
  • Any strength Not Approved
    Pop · All patients
    Total · Yupelri is not indicated for asthma.
Acute Use
0/1 approved regimens
  • Any strength Not Approved
    Pop · Acute bronchospasm / rescue
    Total · Not for acute bronchospasm or rescue. Use a SABA.

For clinical reference only. This workspace is intended for use by qualified healthcare professionals and is not a substitute for clinical judgement, prescribing information, or product monographs. Always verify doses and indications against the most current labelling before prescribing.

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