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COMBIVENT RESPIMAT

SABASAMA SMI

Ipratropium bromide / Albuterol sulfate · Boehringer Ingelheim

Clinical Reference · Data reviewed June 2026

Active Medication & Mechanism

  • Ipratropium bromide SAMA
    20 mcg per actuation

    Short-acting muscarinic antagonist (anticholinergic). Blocks vagal cholinergic tone at M3 receptors, reducing bronchospasm in COPD.

  • Albuterol sulfate SABA
    100 mcg per actuation (albuterol base)

    Short-acting beta2-adrenergic agonist. Relaxes bronchial smooth muscle by stimulating beta2-receptors, providing rapid bronchodilation.

FDA-Approved Dosing — Strength × Indication

20/100 mcg 1 inhalation four times a day (maximum 6 inhalations in 24 hours) → 80/400 mcg (standard); max 120/600 mcg
COPD FDA Approved
Treatment of bronchospasm associated with COPD in patients requiring more than one bronchodilator.
Asthma Not Approved
Combivent Respimat is not indicated for asthma.

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

Approved for as-needed acute use. 1 inhalation as needed; maximum 6 inhalations/24h. The SABA+SAMA combination provides bronchodilation for acute COPD symptoms.

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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