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6/30/2026

Moxifloxacin Injection

Products Affected - Description

    • Moxifloxacin injection, Fresenius Kabi, 400 mg/250 mL, premixed bag, 12 count, NDC 63323-0850-74 - discontinued
    • Moxifloxacin injection, Mylan Institutional (Viatris), 400 mg/250 mL, premixed bag, 12 count, NDC 67457-0323-25

Reason for the Shortage

    • Fresenius Kabi recently discontinued moxifloxacin injection.
    • Viatris did not provide a reason for the shortage. They are sole suppliers of moxifloxacin injection.

Available Products

    • There are no presentations available

Estimated Resupply Dates

    • Viatris has moxifloxacin 400 mg/250 mL premixed bags on back order and the company estimates a release date of mid- to late-November 2026.

Implications for Patient Care

    • Indicated in adult patients for the treatment of community acquired pneumonia, acute bacterial sinusitis, acute bacterial exacerbation of chronic bronchitis, complicated intraabdominal infections, and uncomplicated skin and skin structure infections.[1]
    • Off-label indications: sexually transmitted infections, tuberculosis, surgical prophylaxis, and neutropenic fever.[1]

Safety

    • 1. Could cause tendinitis and tendon rupture. 2. Potential for causing peripheral neuropathy. 3. Exacerbation of Myasthenia Gravis. 4. QT prolongation risk.

Alternative Agents & Management

    • Community acquired pneumonia:[2] 1. First line: amoxicillin 1 g three times daily. 2. Second line: doxycycline 100 mg twice daily. 3. Third line: azithromycin 500 mg on first day then 250 mg daily. 4. Fourth line: moxifloxacin 400 mg once daily, reserved for patients with B-lactam allergy or comorbidities or recent antibiotic exposure. Could also use levofloxacin 750 mg daily for patients with comorbidities/inpatient monotherapy.
    • Acute bacterial sinusitis:[3] 1. First line: amoxicillin with clavulanate 875/125 mg for 5-10 days OR doxycycline 100 mg twice daily for 10 days. 2. Second line: moxifloxacin 400 mg once daily, reserved for patients with B-lactam allergy, severe infection, or failure of first line therapy. Could also use levofloxacin 500-750 mg daily for patients with B-lactam allergy.
    • Acute bacterial exacerbation of chronic bronchitis: (Severe exacerbation) [4] 1. First line: amoxicillin/clavulanate 875/125 mg twice daily. 2. Second line: levofloxacin 750 mg daily. 3. Third line: moxifloxacin 400 mg once daily, reserved if failure of first/second line or allergy/intolerance to them or comorbidities.
    • Complicated intraabdominal infections:[5] 1. First line: cefoxitin 2 grams IV every 6 hours. 2. Second line: ertapenem 1 gram IV every 24 hours. 3. Not usually recommended unless B-lactams are contraindicated or mild-moderate severity, moxifloxacin 400 mg once daily. Could also use ciprofloxacin 400 mg IV every 8-12 hours combined with metronidazole for B-lactam allergy.
    • Skin and skin structure infections: dependent on lab results, moxifloxacin is not the first line agent.

References

    1. Moxifloxacin. Lexicomp Online. Wolters Kluwer Clinical Drug Information. Hudson, Ohio, USA. Accessed; Accessed June 3, 2026.
    2. Metlay JP, Waterer GW, Long AC, et al. Diagnosis and treatment of adults with community-acquired pneumonia. an official clinical practice guideline of the american thoracic society and infectious diseases society of america. American Journal of Respiratory and Critical Care Medicine. 2019;200(7):e45-e67. doi:https://doi.org/10.1164/rccm.201908-1581st
    3. Chow AW, Benninger MS, Brook I, et al. IDSA Clinical Practice Guideline for Acute Bacterial Rhinosinusitis in Children and Adults. Clinical Infectious Diseases. 2012;54(8):e72-e112. doi:https://doi.org/10.1093/cid/cis370
    4. Global Initiative for Chronic Obstructive Lung Disease (GOLD). Global Strategy for the Diagnosis, Management, and Prevention of Chronic Obstructive Pulmonary Disease: 2024 Report. GOLD; 2024. https://goldcopd.org/2024-gold-report/
    5. Robert A Bonomo, Anthony W Chow, Morven S Edwards, Romney Humphries, Pranita D Tamma, Fredrick M Abrahamian, Mary Bessesen, E Patchen Dellinger, Ellie Goldstein, Mary K Hayden, Keith Kaye, Brian A Potoski, Jesús Rodríguez Baño, Robert Sawyer, Marion Skalweit, David R Snydman, Sarah Pahlke, Katelyn Donnelly, Jennifer Loveless, 2024 Clinical Practice Guideline Update by the Infectious Diseases Society of America on Complicated Intra-abdominal Infections: Risk Assessment, Diagnostic Imaging, and Microbiological Evaluation in Adults, Children, and Pregnant People, Clinical Infectious Diseases, 2024;, ciae346, https://doi.org/10.1093/cid/ciae346

Updated

Updated June 30, 2026 by Michelle Wheeler, PharmD, Drug Information Specialist. Created January 13, 2026 by Michelle Wheeler, PharmD, Drug Information Specialist. © 2026, 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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