Albuterol
Active ingredient · 2 therapeutic classes
Sold as AIROMIR · PMS-SALBUTAMOL · VENTOLIN HFA · COMBIVENT UDVS · SALBUTAMOL HFA
- Drug class
- Selective Beta-2-Adrenoreceptor Agonists
- Availability
- Prescription only
- Routes
- Oral, Respiratory (Inhalation), Inhalation, Intravenous
- Markets covered
- 3
- Products on record
- 82
- FDA reports (12 mo)
- 23,205
Overview
Albuterol is an active pharmaceutical ingredient in the Selective Beta-2-Adrenoreceptor Agonists group (R03AC). The information below is compiled per regulator from the product labels on record, with direct links to the original documents.
Regulatory status by market
| Market | Regulator | Products | Last revision |
|---|---|---|---|
| GB United Kingdom | MHRA | 41 | May 29, 2026 |
| US United States | FDA | 25 | April 14, 2026 |
| CA Canada | Health Canada | 16 | June 1, 2026 |
GBUnited Kingdom· MHRA
41 products
Uses
Asmavent® CFC-free Inhaler is indicated in the management of asthma, for the relief of asthma symptoms such as wheezing and shortness of breath, on an as required basis. Asmavent® CFC-free Inhaler should be used to relieve symptoms when they occur and to prevent symptoms in those circumstances recognised by the patient to precipitate an asthma attack, for example before exercise or unavoidable allergen exposure.
Asmavent® CFC-free Inhaler can be used for the relief of symptoms in mild, moderate or severe asthma providing that reliance on the inhaler does not delay the introduction and use of regular inhaled corticosteroid therapy. Asmavent® CFC-free Inhaler may also be used in the treatment of the reversible component of airways obstruction.
How to take
USUnited States· FDA
25 products
Uses
1 INDICATIONS AND USAGE Albuterol Sulfate HFA is a beta 2 -adrenergic agonist indicated for: Treatment or prevention of bronchospasm in adult and pediatric patients aged 4 years and older with reversible obstructive airway disease.
1 ) Prevention of exercise-induced bronchospasm in adult and pediatric patients aged 4 years and older. 1 Bronchospasm Albuterol Sulfate HFA Inhalation Aerosol is indicated for the treatment or prevention of bronchospasm in adult and pediatric patients aged 4 years and older with reversible obstructive airway disease.
2 Exercise-Induced Bronchospasm Albuterol Sulfate HFA is indicated for the prevention of exercise-induced bronchospasm in adult and pediatric patients aged 4 years and older.
How to take
CACanada· Health Canada
16 products
Uses
V. V. Infusion / 1000 mcg/mL sodium chloride, sulphuric acid, and/or sodium hydroxide, water for injection For a complete listing see Dosage Forms, Composition and Packaging section. V. infusion solution is indicated in adults (> 18 years of age) for: the relief of severe bronchospasm associated with acute exacerbations of chronic bronchitis and bronchial asthma, the treatment of status asthmaticus.
In many patients, VENTOLIN® infusion solution will be no more effective, and likely less well tolerated, than VENTOLIN® HFA inhalation aerosol or VENTOLIN® respirator solution. However, patients who are severely ill with airway inflammation and mucus plugging may respond well to parenteral salbutamol after failing to benefit from the inhaled drug.
This product should be administered under the supervision of a qualified health professional who is experienced in the use of parenteral preparations and in the management of asthma. Appropriate management of therapy and complications is only possible when adequate diagnostic and treatment facilities are readily available.
Drug interactions
Known interactions involving Albuterol. Select one for details. This list is informational and not a complete interaction checker.
Showing 240 of 600. Type above to find a specific drug.
Interaction data compiled from DDInter (academic, CC-BY). Severity classification only - this is not a complete interaction checker and not medical advice.
Sources & citations
- [1]MHRA (UK) · PL514630001 · revised November 14, 2025
- [2]FDA DailyMed · 04c8a345-0a0d-5a… · revised December 31, 2024 [PDF]
- [3]Health Canada (DPD) · 02213451 · revised March 22, 2025
- [4]OpenFDA adverse-event reports (US), 12 months ending June 4, 2026.
Information on this page is compiled from public regulatory records. Drugvu is not affiliated with any regulator or pharmaceutical manufacturer. This is not medical advice. Always consult a qualified healthcare professional.