

A clinical guide for providers on Belsomra supply challenges in 2026. Understand availability issues, therapeutic alternatives, and how to help patients.
If your patients are reporting difficulty filling Belsomra (Suvorexant) prescriptions, you're likely dealing with a pattern that has affected prescribers across the country. While Belsomra is not on the FDA's official drug shortage list, real-world availability at the pharmacy level remains inconsistent.
This guide is designed for physicians, nurse practitioners, physician assistants, and other prescribers who need actionable information about Belsomra supply issues and how to manage patients affected by them.
As of early 2026, Belsomra is not listed on the FDA Drug Shortage Database. Merck, the sole manufacturer, has not reported production or distribution disruptions. However, pharmacy-level stockouts are common due to structural factors in the medication's market dynamics.
The key distinction for providers: this is a stocking and distribution challenge, not a manufacturing shortage. The medication exists in the supply chain, but many retail pharmacies do not carry it routinely.
Understanding the root causes helps inform prescribing decisions and patient counseling:
Suvorexant remains under patent protection. Generic versions are not anticipated until 2029–2033. With only one manufacturer and one product, pharmacies cannot source from alternative suppliers, and there is no lower-cost generic version to stock alongside the brand.
Belsomra's wholesale acquisition cost translates to a retail price of approximately $450 to $550 for a 30-day supply. Many pharmacies — particularly independent pharmacies with tighter inventory budgets — avoid stocking high-cost, low-volume brand medications.
Most commercial and government payers subject Belsomra to:
These restrictions reduce the total number of Belsomra prescriptions filled, which further reduces pharmacy stocking motivation.
Controlled substance inventory management requirements add an additional administrative burden. Some pharmacies limit the controlled substances they carry, particularly for lower-volume products.
Despite availability challenges, Belsomra remains a clinically appropriate choice for specific patient populations:
If your patient cannot access Belsomra, two other FDA-approved DORAs may be considered:
Note that availability and payer coverage for these alternatives may be similar to Belsomra. Verify insurance coverage before switching.
For patients where cost or availability is the primary barrier:
When prescribing Belsomra, proactive guidance can prevent treatment interruptions:
MedFinder for Providers allows you to direct patients to pharmacies with real-time Belsomra availability. Consider sharing this resource during the prescribing visit.
If you know a specific pharmacy in your area stocks Belsomra, send the prescription there directly. This saves patients from discovering the stockout after the fact.
Since most payers require PA, consider submitting the authorization at the time of prescribing rather than waiting for a pharmacy rejection. Include documentation of prior medication trials and clinical rationale for Belsomra specifically.
For patients facing cost barriers, direct them to:
For a comprehensive patient-facing resource, refer patients to our guide on saving money on Belsomra.
The availability landscape for Belsomra is unlikely to change significantly until generic Suvorexant enters the market (estimated 2029–2033). Until then, prescribers should:
For more provider-focused resources, visit MedFinder for Providers.
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