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PROVENTIL HFA

SABA MDI

Albuterol sulfate · Kindeva Drug Delivery (distributed by Sandoz)

Clinical Reference · Data reviewed June 2026

Discontinued by manufacturer

Branded Proventil HFA is no longer marketed (Merck exited around September 2021; date approximate). An identical authorized generic (albuterol sulfate inhalation aerosol, manufactured by Kindeva Drug Delivery and distributed by Sandoz) remains available.

Sandoz/Kindeva licensing announcement

Active Medication & Mechanism

  • Albuterol sulfate SABA
    90 mcg albuterol per actuation

    Short-acting beta2-adrenergic agonist. Rapid bronchodilator via beta2-receptor stimulation on airway smooth muscle.

FDA-Approved Dosing — Strength × Indication

90 mcg
Asthma FDA Approved
2 inhalations every 4–6 hours as needed → As needed Treatment or prevention of bronchospasm in patients with reversible obstructive airway disease.
Exercise-Induced Bronchospasm FDA Approved
2 inhalations 15–30 minutes before exercise → As needed Prevention of exercise-induced bronchospasm.

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

Rescue inhaler. Indicated for acute bronchospasm and as-needed symptom relief — onset within minutes. Increasing or frequent use signals worsening asthma control; the label advises reassessment of controller therapy.

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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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