Soma shortage: What providers and prescribers need to know in 2026

Updated:

February 27, 2026

Author:

Peter Daggett

Summarize this blog with AI:

A provider-focused overview of the Carisoprodol (Soma) shortage in 2026, including supply factors, prescribing guidance, and alternative recommendations.

Carisoprodol Supply Disruption: A Provider Briefing for 2026

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.

Understanding the Supply Landscape

Regulatory Constraints

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.

Manufacturer Landscape

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.

Pharmacy-Level Factors

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.

Clinical Considerations for Prescribers

Current Evidence on Carisoprodol

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:

  • Abuse and dependence potential: Carisoprodol is metabolized to Meprobamate, a Schedule IV anxiolytic/sedative with known abuse liability
  • Limited evidence for long-term use: FDA approval is limited to short-term use (up to 2-3 weeks)
  • Drug interaction risks: Significant CNS depression when combined with opioids, benzodiazepines, or alcohol — the so-called "Holy Trinity" combination (Carisoprodol + opioid + benzodiazepine) has been associated with numerous overdose deaths
  • Withdrawal syndrome: Abrupt discontinuation after prolonged use can produce a withdrawal syndrome including insomnia, tremor, anxiety, and in severe cases, seizures

Alternative Agents

When Carisoprodol is unavailable or when clinical circumstances warrant a change, consider the following alternatives:

MedicationTypical DoseKey Considerations
Cyclobenzaprine (Flexeril)5-10 mg TIDMost commonly prescribed muscle relaxant; structurally related to TCAs; avoid in elderly and with MAOIs; not a controlled substance
Methocarbamol (Robaxin)750-1500 mg QID initiallyGenerally well-tolerated; less sedating; good first-line option; not a controlled substance
Tizanidine (Zanaflex)2-8 mg TIDAlpha-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 TIDGABA-B agonist; primarily indicated for spasticity; must taper gradually — abrupt discontinuation can cause seizures; not a controlled substance
Metaxalone (Skelaxin)800 mg TID-QIDLess sedating option; monitor LFTs; may be more expensive; not a controlled substance

Transitioning Patients from Carisoprodol

For patients who have been taking Carisoprodol regularly (particularly at higher doses or for extended periods), abrupt discontinuation is not recommended. Consider:

  • Gradual taper: Reduce dose by 25-50% per week, monitoring for withdrawal symptoms
  • Cross-taper to an alternative: Initiate the new muscle relaxant while tapering Carisoprodol
  • Monitor for withdrawal: Symptoms may include insomnia, nausea, abdominal cramping, headache, and in severe cases, hallucinations or seizures (particularly with Meprobamate accumulation)
  • Patient education: Explain that the switch is driven by supply issues, not a judgment on their treatment history

Helping Patients Navigate Availability

When you prescribe Carisoprodol and your patient reports difficulty filling the prescription:

  1. Recommend MedFinder for Providers — a tool that helps locate pharmacies with specific medications in stock. This can reduce call volume to your office from patients seeking help finding their medication.
  2. Consider calling the pharmacy directly — a provider call can sometimes facilitate orders that patient inquiries cannot.
  3. Explore dosage alternatives — if the 350 mg strength is unavailable, the 250 mg strength may be in stock (and vice versa). Adjusting the prescription may resolve the issue.
  4. Document supply issues — note in the chart that medication changes are driven by supply rather than clinical factors, to maintain continuity of care documentation.

Reporting Shortages

Providers who observe persistent supply issues can report them through:

  • FDA Drug Shortage Staff: fda.gov/drugs/drug-shortages
  • ASHP Drug Shortage Resource Center: Tracks and reports on drug shortages affecting hospital and community pharmacies

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.

Looking Ahead

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.

Additional Resources

Is Carisoprodol still being manufactured in the United States?

Yes. Multiple generic manufacturers continue to produce Carisoprodol, including Mylan (Viatris), Sun Pharmaceutical, Teva, and Par Pharmaceutical. The brand-name product (Soma) has been largely discontinued, but generic supply remains active, though constrained by DEA manufacturing quotas.

What is the recommended approach for transitioning patients off Carisoprodol?

For patients who have been taking Carisoprodol regularly, a gradual taper (reducing dose by 25-50% per week) is recommended to avoid withdrawal symptoms. Cross-tapering to an alternative muscle relaxant while reducing Carisoprodol can help maintain pain control during the transition.

Should I avoid initiating new patients on Carisoprodol given the supply issues?

Given the supply constraints and the availability of effective non-controlled alternatives (Cyclobenzaprine, Methocarbamol, Tizanidine), many providers are choosing to reserve Carisoprodol for patients who have tried and failed other options. This approach is consistent with current clinical guidelines favoring non-controlled first-line agents.

How can I report Carisoprodol supply issues to the appropriate authorities?

Drug shortages can be reported to the FDA Drug Shortage Staff at fda.gov/drugs/drug-shortages and through the ASHP Drug Shortage Resource Center. Reporting helps regulatory agencies understand the true scope of access problems, even when a drug is not officially listed as being in shortage.

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