Albuterol Sulfate (Albuterol Sulfate)

Trade Name : Albuterol Sulfate

Aidarex Pharmaceuticals LLC

SOLUTION

Strength 2.5 mg/3mL

ALBUTEROL SULFATE Adrenergic beta2-Agonists [MoA],beta2-Adrenergic Agonist [EPC]

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Trade Marks displayed in compliance with provisions of: Trademark Act, 1999 u/s 30 and 30 (1) of "Fair use"

GNH India is WHO GDP and ISO 9001 2015 Certified Pharmaceutical Wholesaler/ Supplier/ Exporters/ Importer from India of Albuterol Sulfate (Albuterol Sulfate) which is also known as Albuterol Sulfate and Manufactured by Aidarex Pharmaceuticals LLC. It is available in strength of 2.5 mg/3mL per ml. Read more

Albuterol Sulfate (Albuterol Sulfate) is supplied for Tenders/ Emergency imports/ Un - licensed, Specials, Orphan drug/ Name patient line/ RLD supplies/ Reference listed drugs/ Comparator Drug/ Bio-Similar/ Innovator samples For Clinical trials.  Click to know price.     Read less

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

We deliver your medicines through a validated cold chain shipment process. This process is used as these medicines need to manufactured, transported and stored at very specific temperatures, utilizing thermal and refrigerated packaging methods.

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  • No data
  • Albuterol Sulfate Inhalation Solution 0.083%
  • (Potency expressed as albuterol, equivalent to 3 mg albuterol sulfate)
  • PRESCRIBING INFORMATION
  • FOR INHALATION USE ONLY-NOT FOR INJECTION
  • Albuterol Sulfate Inhalation Solution is a relatively selective beta-adrenergic bronchodilator (seesection below). Albuterol sulfate, the racemic form of albuterol, has the chemical name u03b1-[(-Butylamino)methyl]-4-hydroxy--xylene-u03b1,u03b1'-diol sulfate (2:1) (salt), and the following structural formula:
  • Albuterol sulfate has a molecular weight of 576.70, and the molecular formula (CHNO) u2022 HSO. Albuterol sulfate is a white or practically white powder, freely soluble in water and slightly soluble in alcohol.
  • The World Health Organization recommended name for albuterol base is salbutamol.
  • Albuterol Sulfate Inhalation Solution 0.083% requires no dilution before administration.
  • Each milliliter of Albuterol Sulfate Inhalation Solution 0.083% contains 0.83 mg of albuterol (as 1 mg of albuterol sulfate) in an isotonic, sterile, aqueous solution containing sodium chloride; sulfuric acid is used to adjust the pH to between 3 and 5. Albuterol Sulfate Inhalation Solution 0.083% contains no sulfiting agents or preservatives.
  • Albuterol Sulfate Inhalation Solution is a clear, colorless to light yellow solution.
  • The prime action of beta-adrenergic drugs is to stimulate adenyl cyclase, the enzyme which catalyzes the formation of cyclic-3',5'-adenosine monophosphate (cyclic AMP) from adenosine triphosphate (ATP). The cyclic AMP thus formed mediates the cellular responses. studies andpharmacologic studies have demonstrated that albuterol has a preferential effect on beta-adrenergic receptors compared with isoproterenol. While it is recognized that beta-adrenergic receptors are the predominant receptors in bronchial smooth muscle, 10% to 50% of the beta-receptors in the human heart may be beta-receptors. The precise function of these receptors, however, is not yet established. Albuterol has been shown in most controlled clinical trials to have more effect on the respiratory tract in the form of bronchial smooth muscle relaxation than isoproterenol at comparable doses while producing fewer cardiovascular effects. Controlled clinical studies and other clinical experience have shown that inhaled albuterol, like other beta-adrenergic agonist drugs, can produce a significant cardiovascular effect in some patients, as measured by pulse rate, blood pressure, symptoms, and/or electrocardiographic changes.
  • Albuterol is longer acting than isoproterenol in most patients by any route of administration because it is not a substrate for the cellular uptake processes for catecholamines nor for catechol-O-methyl transferase.
  • Studies in asthmatic patients have shown that less than 20% of a single albuterol dose was absorbed following IPPB (intermittent positive-pressure breathing) or nebulizer administration; the remaining amount was recovered from the nebulizer and apparatus and expired air. Most of the absorbed dose was recovered in the urine 24 hours after drug administration. Following a 3 mg dose of nebulized albuterol, the maximum albuterol plasma level at 0.5 hour was 2.1 ng/mL (range 1.4 to 3.2 ng/mL). There was a significant dose-related response in FEV (forced expiratory volume in one second) and peak flow rate. It has been demonstrated that following oral administration of 4 mg albuterol, the elimination half-life was five to six hours.
  • Animal studies show that albuterol does not pass the blood-brain barrier. Recent studies in laboratory animals (minipigs, rodents, and dogs) recorded the occurrence of cardiac arrhythmias and sudden death (with histologic evidence of myocardial necrosis) when beta-agonists and methylxanthines were administered concurrently. The significance of these findings when applied to humans is currently unknown.
  • In controlled clinical trials, most patients exhibited an onset of improvement in pulmonary function within 5 minutes as determined by FEV. FEV measurements also showed that the maximum average improvement in pulmonary function usually occurred at approximately 1 hour following inhalation of 2.5 mg of albuterol by compressor-nebulizer, and remained close to peak for 2 hours. Clinically significant improvement in pulmonary function (defined as maintenance of a 15% or more increase in FEV over baseline values) continued for 3 to 4 hours in most patients and in some patients continued up to 6 hours.
  • In repetitive dose studies, continued effectiveness was demonstrated throughout the three-month period of treatment in some patients.
  • Published reports of trials in asthmatic children aged 3 years or older have demonstrated significant improvement in either FEV or PEFR within 2 to 20 minutes following single doses of albuterol inhalation solution. An increase of 15% or more in baseline FEV has been observed in children aged 5 to 11 years up to 6 hours after treatment with doses of 0.10 mg/kg or higher of albuterol inhalation solution. Single doses of 3, 4, or 10 mg resulted in improvement in baseline PEFR that was comparable to extent and duration to a 2 mg dose, but doses above 3 mg were associated with heart rate increases of more than 10%.
  • Albuterol sulfate inhalation solution is indicated for the relief of bronchospasm in patients 2 years of age and older with reversible obstructive airway disease and acute attacks of bronchospasm.
  • Albuterol sulfate inhalation solution is contraindicated in patients with a history of hypersensitivity to any of its components.
  • As with other inhaled beta-adrenergic agonists, albuterol sulfate inhalation solution can produce paradoxical bronchospasm, which can be life threatening. If it occurs, the preparation should be discontinued immediately and alternative therapy instituted.
  • Fatalities have been reported in association with excessive use of inhaled sympathomimetic drugs and with the home use of nebulizers. It is, therefore, essential that the physician instruct the patient in the need for further evaluation, if his/her asthma becomes worse. In individual patients, any beta-adrenergic agonist, including albuterol solution for inhalation, may have a clinically significant cardiac effect.
  • Immediate hypersensitivity reactions may occur after administration of albuterol as demonstrated by rare cases of urticaria, angioedema, rash, bronchospasm, and oropharyngeal edema.
  • No data
  • No data
  • Manifestations of overdosage may include seizures, anginal pain, hypertension, hypokalemia, tachycardia with rates up to 200 beats/min, and exaggeration of the pharmacological effects listed in. In isolated cases in children 2 to 12 years of age, tachycardia with rates >200 beats/min has been observed.
  • The oral LD in rats and mice was greater than 2,000 mg/kg. The inhalational LD could not be determined.
  • There is insufficient evidence to determine if dialysis is beneficial for overdosage of albuterol inhalation solution.
  • The usual dosage for adults and for children weighing at least 15 kg is 2.5 mg of albuterol (one vial) administered three to four times daily by nebulization. Children weighing < 15 kg who require < 2.5 mg/dose (i.e., less than a full vial) should use albuterol inhalation solution, 0.5% instead of albuterol inhalation solution, 0.083%. More frequent administration or higher doses are not recommended. To administer 2.5 mg of albuterol, administer the entire contents of one sterile unit dose vial (3 mL of 0.083% inhalation solution) by nebulization. The flow rate is regulated to suit the particular nebulizer so that albuterol inhalation solution will be delivered over approximately 5 to 15 minutes.
  • The use of albuterol sulfate inhalation solution can be continued as medically indicated to control recurring bouts of bronchospasm. During this time most patients gain optimum benefit from regular use of the inhalation 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.
  • Unit-dose plastic vial containing Albuterol Sulfate Inhalation Solution 0.083%, 2.5 mg/3 mL. Equivalent to 0.5 mL albuterol (as the sulfate) 0.5% (2.5 mg albuterol) diluted to 3 mL. Supplied in cartons as listed below.
  • NDC 33261-0789-01 25 vials per carton / 25 vials per foil pouch
  • PROTECT FROM LIGHT. Store in pouch until time of use. Store between 2u00b0 and 25u00b0 C (36u00b0 and 77u00b0 F).
  • Rx only.
  • Manufactured by:
  • To report SUSPECTED ADVERSE REACTIONS, contact Ritedose
  • Pharmaceuticals, LLCat 1-855-806-3300 or FDAat 1-800-FDA-1088 or n
  • RPIN0032October 2012
  • Repackaged By :Aidarex Pharmaceuticals LLC,Corona, CA 92880
  • Albuterol Sulfate Inhalation Solution 0.083%n
  • Note: This is a unit-dose vial. No dilution is required.
  • Read complete instructions carefully before using.
  • Note: Use only as directed by your physician. More frequent administration or higher doses are not recommended
  • Store Albuterol Sulfate Inhalation Solution 0.083% between 2u00b0 and 25u00b0 C (36u00b0 and 77u00b0 F). Store in pouch until time of use.
  • ADDITIONAL INSTRUCTIONS: n
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  • Manufactured by:
  • To report SUSPECTED ADVERSEREACTIONS, contact RitedosePharmaceuticals, LLC at 1-855-806-3300 or FDAat 1-800-FDA-1088 or n
  • RPIN0032October 2012
  • Repackaged By :Aidarex Pharmaceuticals LLC,Corona, CA 92880
  • NDC 33261-0789-01
  • Albuterol SulfateInhalation Solution, 0.083%*
  • 2.5 mg / 3 mL*
  • *Potency expressed as albuterol, equivalent to 3 mg albuterol sulfate.
  • Each mL contains 1 mg albuterol sulfate, equivalent to 0.83 mg albuterolin an aqueous solution containing sodium chloride and sulfuric acid to adjust pH between 3 and 5. Contains no preservatives.Please consult your physician before use. Do not exceed recommended dosage.n See package insert. n n Discard if solution becomes discolored.(Note: Albuterol Sulfate Inhalation Solution is a clear, colorless to light yellow solution.)
  • Rx Only
  • Arrayn- 25 x 3 mL Sterile Unit-Dose Vials

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