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2/27/2024

Albuterol Inhalation Solution

Products Affected - Description

    • Albuterol Sulfate inhalation solution, Akorn, 0.5% 5 mg/mL, 20 mL bottle, 1 count, NDC 50383-0741-20 - discontinued

Reason for the Shortage

    • Akorn ceased operations in February 2023.
    • Mylan (Viatris) has albuterol sulfate inhalation solution available.
    • Nephron Pharmaceuticals has albuterol sulfate inhalation solution available.
    • Ritedose has albuterol sulfate inhalation solution available.
    • Sun Pharma has albuterol sulfate inhalation solution available.

Available Products

    • Albuterol Sulfate inhalation solution, Mylan (Viatris), 0.083% 3 mL (2.5 mg), Unit-of-use vial, 25 vials per foil pouch, 25 count, NDC 00378-8270-52
    • Albuterol Sulfate inhalation solution, Mylan (Viatris), 0.083% 3 mL (2.5 mg), Unit-of-use vial, 30 vials per foil pouch, 30 count, NDC 00378-8270-93
    • Albuterol Sulfate inhalation solution, Mylan (Viatris), 0.083% 3 mL (2.5 mg), Unit-of-use vial, 1 vial per foil pouch 30 count, NDC 00378-8270-55
    • Albuterol Sulfate inhalation solution, Mylan (Viatris), 0.083% 3 mL (2.5 mg), Unit-of-use vial, 30 vials per foil pouch 60 count, NDC 00378-8270-91
    • Albuterol Sulfate inhalation solution, Nephron Pharmaceuticals Corporation, 0.5% 2.5 mg/0.5 mL, Unit-of-use vial, 30 count, NDC 00487-9901-30
    • Albuterol Sulfate inhalation solution, Nephron Pharmaceuticals Corporation, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 25 count, NDC 00487-9501-25
    • Albuterol Sulfate inhalation solution, Nephron Pharmaceuticals Corporation, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 1 vial per foil pouch, 30 count, NDC 00487-9501-01
    • Albuterol Sulfate inhalation solution, Nephron Pharmaceuticals Corporation, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 30 count, NDC 00487-9501-03
    • Albuterol Sulfate inhalation solution, Ritedose, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 25 vials per foil pouch, 25 count, NDC 76204-0200-25
    • Albuterol Sulfate inhalation solution, Ritedose, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 1 vial per foil pouch, 30 count, NDC 76204-0200-01
    • Albuterol Sulfate inhalation solution, Ritedose, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 30 vials per foil pouch, 30 count, NDC 76204-0200-30
    • Albuterol Sulfate inhalation solution, Ritedose, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 2 pouches of 30 vials, 60 count, NDC 76204-0200-60
    • Albuterol Sulfate inhalation solution, Sun Pharma, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 5 vials per foil pouch, 30 count, NDC 47335-0703-52
    • Albuterol Sulfate inhalation solution, Sun Pharma, 0.083% 3 mL (2.5 mg), Unit-of-use vial, 5 vials per foil pouch, 60 count, NDC 47335-0703-54

Alternative Agents & Management

    • Levalbuterol hydrochloride inhalation solution may be used as an alternative to albuterol inhalation solution. Most levalbuterol inhalation solution presentations are currently available.
    • Levalbuterol solution for nebulization is labeled for the management of acute bronchospasm in adults, adolescents, and children 6 years of age and older with reversible obstructive airway disease.[1]
    • In children 6-11 years of age, the initial dose is 0.31 mg nebulized three times daily. Routine dosing should not exceed 0.63 mg three times daily.[1]
    • In adults or adolescents 12 years of age or older, the initial dose is 0.63 mg nebulized three times daily (every 6 to 8 hours). Patients 12 years of age and older with more severe asthma or those not responding adequately to the 0.63 mg dose may benefit from 1.25 mg nebulized three times a day.[1]

References

    1. Lexicomp online, AHFS Drug Information (Adult and Pediatric). Bethesda, MD: American Society of Health-System Pharmacists; 2022.

Updated

Updated February 27, 2024 by Leslie Jensen, PharmD, Drug Information Specialist. Created March 29, 2022 by Leslie Jensen, PharmD, Drug Information Specialist. © 2024, Drug Information Service, University of Utah, Salt Lake City, UT.

Disclaimer

Drug Shortage Bulletins are copyrighted by the Drug Information Service of the University of Utah and provided by ASHP as its exclusive authorized distributor. ASHP and the University of Utah make no representations or warranties, express or implied, including, but not limited to, any implied warranty of merchantability and/or fitness for a particular purpose, with respect to such information, and specifically disclaim all such warranties. Users of this information are advised that decisions regarding the use of drugs and drug therapies are complex medical decisions and that in using this information, each user must exercise his or her own independent professional judgment. Neither ASHP nor the University of Utah assumes any liability for persons administering or receiving drugs or other medical care in reliance upon this information, or otherwise in connection with this Bulletin. Neither ASHP nor the University of Utah endorses or recommends the use of any particular drug. Any application of this information for any purpose shall be limited to personal, non-commercial use.

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