

A provider-focused overview of the Carisoprodol (Soma) shortage in 2026, including supply factors, prescribing guidance, and alternative recommendations.
Providers across the country are hearing from patients who cannot fill their Carisoprodol (Soma) prescriptions. While not listed as an active shortage on the FDA's drug shortage database as of early 2026, the practical reality is that many pharmacies — particularly large chain pharmacies — are unable to reliably stock this medication. This article provides an overview of the supply situation and clinical guidance for managing affected patients.
Carisoprodol is classified as a Schedule IV controlled substance under the Controlled Substances Act. The DEA establishes annual Aggregate Production Quotas (APQs) and individual manufacturing quotas that limit how much Carisoprodol can be produced domestically. These quotas are based on estimated medical need, research requirements, and historical usage patterns.
As prescribing trends for Carisoprodol have declined — driven by clinical guidelines that increasingly favor non-controlled alternatives — the DEA has adjusted quotas accordingly. This creates a feedback loop: lower quotas mean less manufacturing capacity, which can lead to spot shortages even when overall demand has decreased.
The brand-name product (Soma, originally marketed by MedPointe/Meda Pharmaceuticals) has been largely discontinued. Generic Carisoprodol remains available from several manufacturers including Mylan (Viatris), Sun Pharmaceutical, Teva, and Par Pharmaceutical (Endo). However, consolidation in the generic pharmaceutical industry means fewer production lines and less redundancy when disruptions occur.
Many pharmacy chains have implemented controlled substance stocking algorithms that may deprioritize medications with higher abuse potential or declining prescription volumes. Individual pharmacies may carry limited quantities of Carisoprodol, and some locations may not stock it at all. Independent pharmacies generally have more flexibility in their ordering practices.
It is worth noting the clinical context around Carisoprodol prescribing. The American Academy of Orthopaedic Surgeons (AAOS) and other professional organizations have generally moved away from recommending Carisoprodol as a first-line agent for acute musculoskeletal pain due to:
When Carisoprodol is unavailable or when clinical circumstances warrant a change, consider the following alternatives:
| Medication | Typical Dose | Key Considerations |
|---|---|---|
| Cyclobenzaprine (Flexeril) | 5-10 mg TID | Most commonly prescribed muscle relaxant; structurally related to TCAs; avoid in elderly and with MAOIs; not a controlled substance |
| Methocarbamol (Robaxin) | 750-1500 mg QID initially | Generally well-tolerated; less sedating; good first-line option; not a controlled substance |
| Tizanidine (Zanaflex) | 2-8 mg TID | Alpha-2 agonist; effective for spasticity and acute spasm; monitor LFTs; significant CYP1A2 interactions (ciprofloxacin, fluvoxamine contraindicated); not a controlled substance |
| Baclofen (Lioresal) | 5-20 mg TID | GABA-B agonist; primarily indicated for spasticity; must taper gradually — abrupt discontinuation can cause seizures; not a controlled substance |
| Metaxalone (Skelaxin) | 800 mg TID-QID | Less sedating option; monitor LFTs; may be more expensive; not a controlled substance |
For patients who have been taking Carisoprodol regularly (particularly at higher doses or for extended periods), abrupt discontinuation is not recommended. Consider:
When you prescribe Carisoprodol and your patient reports difficulty filling the prescription:
Providers who observe persistent supply issues can report them through:
Reporting helps regulatory agencies understand the true scope of access problems, particularly for medications like Carisoprodol where supply may be technically adequate at the national level but practically unavailable in many communities.
The availability landscape for Carisoprodol is unlikely to improve substantially in the near term. The combination of declining prescribing trends, DEA quota adjustments, and pharmacy stocking policies suggests that access challenges will persist. Providers should be prepared to counsel patients on alternatives and have transition plans ready for patients who cannot find their medication.
For additional clinical resources and tools to help your patients, visit MedFinder for Providers. For a complementary guide on helping patients navigate cost barriers, see How to help your patients find Soma in stock.
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