Auvelity XR Shortage: What Providers and Prescribers Need to Know in 2026

Updated:

February 27, 2026

Author:

Peter Daggett

Summarize this blog with AI:

A provider briefing on Auvelity XR availability in 2026. Current supply status, prior authorization landscape, prescribing considerations, and tools to help patients access their medication.

Auvelity XR Shortage: What Providers and Prescribers Need to Know in 2026

If you prescribe Auvelity XR (dextromethorphan/bupropion extended-release), you're likely fielding questions from patients who can't find it at their pharmacy. This provider briefing covers the current supply landscape, payer dynamics, and practical tools to help your patients maintain access to their medication.

Complete Timeline: How We Got Here

August 2022: The FDA approved Auvelity (dextromethorphan HBr/bupropion HCl) for the treatment of major depressive disorder in adults, making it the first oral NMDA receptor antagonist approved for MDD.

Late 2022 – 2023: Axsome Therapeutics launched Auvelity commercially. Initial uptake was gradual as payer coverage policies were established and prescriber awareness grew. Early adopters were primarily psychiatrists treating patients with inadequate response to SSRIs and SNRIs.

2024: Prescribing volume increased substantially as clinical data and real-world experience reinforced efficacy signals from the GEMINI and ASCEND trials. Payer coverage expanded but remained inconsistent, with most plans requiring prior authorization and step therapy.

2025: Axsome introduced the extended-release formulation (Auvelity XR), improving dosing convenience. Growing prescriber adoption led to increased demand, particularly in metropolitan areas with high psychiatry density.

Early 2026: Auvelity XR is not on the FDA drug shortage list. However, localized availability gaps persist due to pharmacy stocking patterns and wholesaler allocation dynamics.

Current Availability Landscape for Prescribers

Supply Chain Status

Axsome Therapeutics reports adequate manufacturing capacity for current demand. The supply chain from manufacturer to wholesaler is intact. The bottleneck occurs at the pharmacy level, where stocking decisions create a patchwork of availability.

Prior Authorization Complexity

Prior authorization remains a significant barrier to patient access. The current payer landscape includes:

  • Commercial plans: Most require PA with documentation of inadequate response to 1-2 first-line antidepressants (typically SSRIs/SNRIs). Step therapy requirements vary by plan.
  • Medicare Part D: Coverage varies by plan. Many formularies place Auvelity XR on Tier 3 or specialty tier with PA required. Some plans have adopted more restrictive step therapy (2-3 prior agents).
  • Medicaid: State-by-state variation. Some state Medicaid programs have added Auvelity XR to their preferred drug lists; others maintain strict PA requirements.

Indication-Specific Coverage

Coverage approval rates are highest when documentation clearly supports:

  • Diagnosis of MDD with documented treatment failures
  • Specific agents tried, doses, and duration of adequate trials
  • Clinical rationale for Auvelity XR's novel mechanism (NMDA antagonism) versus continued serotonergic therapy

The Real-World Availability Picture

Supply Chain Mechanics

Understanding the manufacturer → wholesaler → pharmacy pipeline helps explain why patients encounter availability gaps:

  • Manufacturer (Axsome): Producing adequate supply
  • Wholesalers (McKesson, Cardinal Health, AmerisourceBergen): Distributing to pharmacies with allocation systems that may limit quantities for pharmacies without established ordering history
  • Pharmacies: Making individual stocking decisions based on demand, cost ($900-$1,300 wholesale per month of therapy), and inventory risk

Dose-Specific Variation

The standard 45 mg/105 mg strength is the most readily available. Pharmacies that stock Auvelity XR typically carry this formulation, as it covers both the titration and maintenance phases.

Regional Disparities

Availability tends to be better in urban and suburban areas with higher concentrations of psychiatry practices and specialty pharmacies. Rural areas may have more limited access, making medication finder services and mail-order options particularly valuable for these patients.

Cost and Access: The Numbers Your Patients Are Seeing

List Price

The wholesale acquisition cost (WAC) for Auvelity XR places the retail cash price at approximately $900-$1,300 per month for most patients paying out of pocket.

Savings Programs

The Auvelity Savings Card from Axsome reduces the copay to as little as $10 per fill for eligible commercially insured patients. This program has been critical for patient retention. Enrollment is available at auvelity.com/savings.

Medicare and Medicaid Coverage

Medicare Part D patients are not eligible for the manufacturer copay card (per federal anti-kickback statute). Their out-of-pocket costs depend entirely on plan tier placement and coverage phase. Medicaid coverage varies by state, with some programs offering more favorable access than others.

Patient Assistance Programs

The Axsome Patient Assistance Program provides Auvelity XR at no cost for qualifying uninsured or underinsured patients. Providers can help patients apply through the Axsome support portal or direct patients to resources like NeedyMeds and RxAssist.

Tools and Resources for Your Practice

  • Medfinder Provider Portal — Search for pharmacies with Auvelity XR in stock on behalf of your patients. Saves clinical staff time and improves patient follow-through.
  • FDA Drug Shortage Database — Monitor official shortage status at accessdata.fda.gov
  • Auvelity Savings and Supportauvelity.com/savings for copay card enrollment and PAP applications
  • Axsome Medical Affairs — Available for clinical questions about Auvelity XR prescribing and coverage

Looking Ahead

Several developments may impact Auvelity XR access in the coming months:

  • Manufacturing scale-up: Axsome has indicated plans to expand production capacity in response to growing demand
  • Payer policy evolution: As real-world evidence accumulates, some payers may relax step therapy requirements or improve tier placement
  • Pharmacy stocking: As prescribing volume increases and stabilizes, more pharmacies will find it economically viable to stock Auvelity XR regularly
  • Generic timeline: No near-term generic competition expected due to patent protection, meaning brand access optimization remains critical

Final Thoughts

As prescribers, you are uniquely positioned to advocate for your patients' access to Auvelity XR. Understanding the supply chain dynamics, payer landscape, and available support programs enables you to proactively address access barriers before they lead to treatment interruptions.

Key actions for your practice:

  1. Use the Medfinder provider portal to help patients locate pharmacies with Auvelity XR in stock
  2. Ensure patients are enrolled in the Auvelity Savings Card program before their first fill
  3. Document treatment history thoroughly to streamline prior authorization approvals
  4. Build relationships with pharmacies that reliably stock Auvelity XR

Related resources for providers:

Share this patient-facing update with your patients: Auvelity XR Shortage Update for Patients

Is Auvelity XR still on the FDA shortage list in 2026?

No, Auvelity XR is not currently listed on the FDA drug shortage database as of early 2026. Axsome Therapeutics reports adequate manufacturing capacity. The availability challenges patients experience are localized and driven by pharmacy-level stocking decisions and wholesaler allocation dynamics.

Why are my patients still having trouble filling Auvelity XR prescriptions?

The primary barriers are pharmacy-level: many pharmacies don't stock Auvelity XR due to its high wholesale cost and uncertain demand. Wholesaler allocation limits can also delay new orders. Using the Medfinder provider portal can help locate pharmacies with stock for your patients.

What prior authorization documentation is most effective for Auvelity XR?

Document specific prior antidepressant trials including agent names, doses, duration of adequate trials, and reasons for discontinuation. Include clinical rationale for Auvelity XR's novel NMDA receptor mechanism, particularly for patients with inadequate response to serotonergic agents.

What alternatives should I consider if a patient cannot access Auvelity XR?

Consider bupropion (Wellbutrin XL) as a partial mechanistic substitute, esketamine (Spravato) for patients with treatment-resistant depression who can access REMS sites, or vortioxetine (Trintellix) for patients with cognitive symptoms. SSRIs/SNRIs remain appropriate first-line options for treatment-naive patients.

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