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Salbutamol
Albuterol

Salbutamol Sulfate grades are available to suit formulations that require rapid and direct drug delivery

HUMAN API

Salbutamol

Salbutamol is a crucial Active Pharmaceutical Ingredient (API) belonging to the class of Short-Acting Beta-2 Agonists (SABA). It is the most commonly used "reliever" medication for treating acute asthma attacks and bronchospasm. We supply Salbutamol (typically as the Sulfate salt) in ultra-pure grades, suitable for complex formulations such as inhalers and nebulizer solutions.

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).
A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.
A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.
Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).
Therapeutic Class:
Bronchodilator.
Mechanism of Action:
Selectively stimulates Beta-2 receptors in the smooth muscles of the bronchial tubes, leading to rapid muscle relaxation and bronchodilation (widening of the airways).
Clinical Application:
Treatment of acute asthma exacerbations, prevention of exercise-induced bronchospasm, and management of Chronic Obstructive Pulmonary Disease (COPD).
Competitive Advantage:
Fast onset of action and high efficacy as an emergency "rescue" bronchodilator, ensuring consistent market demand.
Inhalers

Metered Dose Inhalers (MDIs) and Dry Powder Inhalers (DPIs).

Supplied in precisely controlled Micronized Grade particle sizes for optimal lung distribution.

Nebulizer Solutions

Sterile aqueous solutions for use in nebulizer devices.

Excellent solubility of the Sulfate salt and stability in sterile aqueous solutions.

Oral Formulations

Immediate- and extended-release tablets, and syrups.

High API quality ensures stability and good tolerance in both liquid and solid oral formulations.

Regulatory Compliance

The product conforms to the specified requirements of the United States Pharmacopeia (USP), European Pharmacopoeia (EP), and/or British Pharmacopoeia (BP).

Certificate of Analysis (CoA)

A detailed CoA is issued with every batch, outlining potency, purity profile, and microbiological testing verification.

Drug Master File (DMF)

A comprehensive Drug Master File is available to support registration submissions to regulatory authorities worldwide.

Manufacturing Operations

Production takes place in certified facilities that strictly adhere to current Good Manufacturing Practices (cGMP).

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