Drug Facts
Composition & Profile
Identifiers & Packaging
HOW SUPPLIED Albuterol Sulfate Inhalation Solution, 2.5 mg/0.5 mL (equivalent to 3 mg albuterol sulfate), is a clear, colorless to light yellow solution, and is supplied in plastic sterile unit-dose vials of 0.5 mL each, supplied in individual foil pouches: NDC 76204-027-01: 30 unit-dose vials, each in an individual pouch. Storage and Handling Store between 2°C and 25°C (36°F – 77°F). Protect from light. Store in a pouch until time of use. Rx Only Manufactured for: Ritedose Pharmaceuticals, LLC Columbia, SC 29203 Manufactured by: The Ritedose Corporation Columbia, SC 29203 March 2024; Albuterol Sulfate Inhalation Solution, 0.5% Foil Pouch (1 Count) updated-rdp-albuterol-1ct-foil; Albuterol Sulfate Inhalation Solution, 0.5% Carton (30 Count) rdp-albuterol-carton-30ct
- HOW SUPPLIED Albuterol Sulfate Inhalation Solution, 2.5 mg/0.5 mL (equivalent to 3 mg albuterol sulfate), is a clear, colorless to light yellow solution, and is supplied in plastic sterile unit-dose vials of 0.5 mL each, supplied in individual foil pouches: NDC 76204-027-01: 30 unit-dose vials, each in an individual pouch. Storage and Handling Store between 2°C and 25°C (36°F – 77°F). Protect from light. Store in a pouch until time of use. Rx Only Manufactured for: Ritedose Pharmaceuticals, LLC Columbia, SC 29203 Manufactured by: The Ritedose Corporation Columbia, SC 29203 March 2024
- Albuterol Sulfate Inhalation Solution, 0.5% Foil Pouch (1 Count) updated-rdp-albuterol-1ct-foil
- Albuterol Sulfate Inhalation Solution, 0.5% Carton (30 Count) rdp-albuterol-carton-30ct
Overview
Albuterol Sulfate Inhalation Solution, 0.5% contains albuterol sulfate, USP, the racemic form of albuterol and a relatively selective beta 2 - adrenergic bronchodilator. Albuterol sulfate has the chemical name α 1 [(tert-Butylamino) methyl]-4-hydroxy-m-xylene-α, α’-diol sulfate (2:1) (salt), and the following chemical structure: The molecular weight of albuterol sulfate is 576.7, and the empirical formula is (C 13 H 21 NO 3 ) 2 • H 2 SO 4 . Albuterol sulfate is a white crystalline powder, soluble in water and slightly soluble in ethanol. The World Health Organization’s recommended name for albuterol base is salbutamol. Albuterol sulfate inhalation solution, 0.5%, is in concentrated form. Dilute 0.5 mL of the solution to 3 mL with sterile normal saline solution prior to administration by nebulization. Each 0.5 mL Unit-Dose Vial Contains: 2.5 mg of albuterol (equivalent to 3 mg of albuterol sulfate, USP) in a sterile, aqueous solution; sulfuric acid is used to adjust the pH to between 3 and 5. Albuterol Sulfate Inhalation solution contains no sulfiting agents or preservatives. It is supplied in 0.5 mL sterile Unit-Dose Vials. Albuterol sulfate inhalation solution is a clear, colorless to light yellow solution. chemical-structure
Indications & Usage
Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 12 years of age and older with reversible obstructive airway disease and acute attacks of bronchospasm.
Dosage & Administration
The usual dosage for adults and pediatric patients 12 years of age and older is 2.5 mg of albuterol (one unit-of-use vial) administered 3 to 4 times daily by nebulization. More frequent administration or higher doses are not recommended. To administer 2.5 mg of albuterol, dilute 0.5 mL of the 0.5% solution for inhalation to a total volume of 3 mL with sterile normal saline solution and administer by nebulization. The flow rate is regulated to suit the particular nebulizer so that albuterol sulfate inhalation solution will be delivered over approximately 5 to 15 minutes. Drug compatibility (physical and chemical), efficacy, and safety of albuterol sulfate inhalation solution when mixed with other drugs in a nebulizer have not been established. The use of albuterol sulfate inhalation solution can be continued as medically indicated to control recurring bouts of bronchospasm. During treatment, most patients gain optimum benefit from regular use of the nebulizer solution. If a previously effective dosage regimen fails to provide the usual relief, medical advice should be sought immediately, as this is often a sign of seriously worsening asthma which would require reassessment of therapy. The nebulizer should be cleaned in accordance with the manufacturer’s instructions. Failure to do so could lead to bacterial contamination of the nebulizer and possible infection.
Warnings & Precautions
WARNINGS DETERIORATION OF ASTHMA Asthma may deteriorate acutely over a period of hours or chronically over several days or longer. If the patient needs more doses of albuterol sulfate inhalation solution than usual, this may be a marker of destabilization of asthma and requires re-evaluation of the patient and treatment regimen, giving special consideration to the possible need for anti-inflammatory treatment, e.g., corticosteroids. USE OF ANTI-INFLAMMATORY AGENTS The use of beta-adrenergic agonist bronchodilators alone may not be adequate to control asthma in many patients. Early consideration should be given to adding anti-inflammatory agents, e.g., corticosteroids. PARADOXICAL BRONCHOSPASM Albuterol sulfate inhalation solution can produce paradoxical bronchospasm, which may be life threatening. If paradoxical bronchospasm occurs, albuterol sulfate inhalation solution should be discontinued immediately and alternative therapy instituted. It should be recognized that paradoxical bronchospasm, when associated with inhaled formulations, frequently occurs with the first use of a new vial. CARDIOVASCULAR EFFECTS Albuterol sulfate inhalation solution, like all other beta-adrenergic agonists, can produce a clinically significant cardiovascular effect in some patients as measured by pulse rate, blood pressure, and/or symptoms. Although such effects are uncommon after administration of albuterol sulfate inhalation solution at recommended doses, if they occur, the drug may need to be discontinued. In addition, beta-agonists have been reported to produce electrocardiogram (ECG) changes, such as flattening of the T wave, prolongation of the QTc interval, and ST segment depression. The clinical significance of these findings is unknown. Therefore, albuterol sulfate inhalation solution, like all sympathomimetic amines, should be used with caution in patients with cardiovascular disorders, especially coronary insufficiency, cardiac arrhythmias, and hypertension. IMMEDIATE HYPERSENSITIVITY REACTIONS Immediate hypersensitivity reactions may occur after administration of albuterol, as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, anaphylaxis, and oropharyngeal edema.
Contraindications
Albuterol sulfate inhalation solution is contraindicated in patients with a history of hypersensitivity to albuterol or any of its components.
Adverse Reactions
The results of clinical trials with albuterol sulfate inhalation solution in 135 patients showed the following side effects which were considered probably or possibly drug related: Percent Incidence of Adverse Reactions Reaction Percent Incidence (N=135) Central Nervous System Tremors 20 Dizziness 7 Nervousness 4 Headache 3 Insomnia 1 Gastrointestinal Nausea 4 Dyspepsia 1 Ear, nose and throat Nasal congestion 1 Pharyngitis <1 Cardiovascular Tachycardia 1 Hypertensions 1 Respiratory Bronchospasm 8 Cough 4 Bronchitis 4 Wheezing 1 No clinically relevant laboratory abnormalities related to albuterol sulfate inhalation solution were determined in these studies. Cases of urticaria, angioedema, rash, bronchospasm, hoarseness, oropharyngeal edema, and arrhythmias (including atrial fibrillation, supraventricular tachycardia, and extrasystoles) have also been reported after the use of inhaled albuterol. To report SUSPECTED ADVERSE REACTIONS, contact Ritedose Pharmaceuticals, LLC at 1-855-806-3300 or FDA at 1-800-FDA-1088 or www.fda.gov/medwatch .
Drug Interactions
Other short-acting sympathomimetic aerosol bronchodilators or epinephrine should not be used concomitantly with albuterol sulfate inhalation solution.
Storage & Handling
Storage and Handling Store between 2°C and 25°C (36°F – 77°F). Protect from light. Store in a pouch until time of use. Rx Only Manufactured for: Ritedose Pharmaceuticals, LLC Columbia, SC 29203 Manufactured by: The Ritedose Corporation Columbia, SC 29203 March 2024
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