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COMBIVENT RESPIMAT

Albuterol/Ipratropium

COMBIVENT RESPIMAT

SABASAMA SMI

Ipratropium bromide / Albuterol sulfate · Boehringer Ingelheim

Clinical Reference

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 by Indication

// approval varies by strength + age
COPD
1/1 approved regimens
  • 20/100 mcg FDA Approved
    Pop · Adults (≥18 years)
    1 inhalation four times a day (maximum 6 inhalations in 24 hours)
    Treatment of bronchospasm associated with COPD in patients requiring more than one bronchodilator.
    Total · 80/400 mcg (standard); max 120/600 mcg
Asthma
0/1 approved regimens
  • Any strength Not Approved
    Pop · All patients
    Total · Combivent Respimat is not indicated for asthma.
Acute Use
1/1 approved regimens
  • 20/100 mcg FDA Approved
    Pop · Adults with COPD
    1 inhalation as needed; maximum 6 inhalations/24h
    The SABA+SAMA combination provides bronchodilation for acute COPD symptoms.
    Total · Maximum 120/600 mcg

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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