Updated: January 19, 2026
Disulfiram Shortage: What Providers and Prescribers Need to Know in 2026
Author
Peter Daggett

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The disulfiram shortage is impacting AUD patients' access to medication. Providers need to know which presentations are unavailable and how to support patients through the gap.
Prescribers managing patients on disulfiram for alcohol use disorder (AUD) are increasingly encountering a supply problem that began in mid-2024. One or more commercial presentations of disulfiram tablets remain unavailable, and patients are calling with reports of empty pharmacy shelves, rejected prescriptions, and confusion about what to do next.
This guide is written specifically for clinicians — including primary care physicians, psychiatrists, addiction medicine specialists, NPs, and PAs — prescribing disulfiram or considering it as part of a medication-assisted treatment (MAT) plan. It covers shortage status, clinical implications, transitioning strategies, and tools to help your patients maintain access to care.
Shortage Status and Affected Presentations
The ASHP Drug Shortage database first listed disulfiram in July 2024 and updated the entry in May 2025 — indicating the shortage had persisted for over a year with no firm resolution timeline. The affected presentations include:
- Chartwell disulfiram 500 mg tablet (NDC 62135-0432-90) — confirmed unavailable
- At least one Alvogen presentation — unavailable, no resupply date confirmed
Four total presentations of disulfiram tablets are marketed in the U.S. The shortage does not affect all presentations equally, meaning that a patient's ability to fill their prescription depends heavily on which manufacturer's product their pharmacy stocks.
Clinical Background: Disulfiram's Role in AUD Treatment
Disulfiram is an aldehyde dehydrogenase (ALDH2) inhibitor that irreversibly blocks the metabolism of acetaldehyde, a toxic alcohol breakdown product. When alcohol is consumed, acetaldehyde builds up to 5-10 times normal levels, producing the disulfiram-alcohol reaction (DAR): flushing, nausea, vomiting, tachycardia, dyspnea, hypotension, and in severe cases, cardiac events and death.
Per the APA's 2018 Clinical Practice Guideline for AUD, disulfiram is a second-line option, recommended when naltrexone and acamprosate are contraindicated or ineffective. Optimal candidates are motivated, have social supports that can supervise administration, have no significant hepatic or cardiac disease, and do not have active psychotic disorders. Because disulfiram requires full informed consent and reliable compliance monitoring, it is most effective in structured treatment settings.
Transitioning Patients Off Disulfiram: Clinical Considerations
If a patient cannot fill disulfiram due to the shortage, the following transition considerations apply:
- Naltrexone (oral or injectable): First-line per guidelines; reduces cravings via mu-opioid receptor antagonism. Contraindicated in patients actively using opioids or with acute hepatitis (LFTs >3-5x ULN). Wait at least 7-10 days after last opioid use before initiating. No washout needed from disulfiram for naltrexone; however, if transitioning directly, confirm no alcohol ingestion for safety.
- Acamprosate: First-line; modulates GABA-A and NMDA glutamate receptors. Not hepatically metabolized — well-suited for patients with liver disease. Initiate once abstinence is established. Dose: 666 mg TID.
- Combination therapy: Naltrexone + acamprosate is supported by evidence (COMBINE trial) and may be appropriate for patients with severe AUD who need robust pharmacological support.
Key Drug Interactions and Contraindications to Review
Before prescribing disulfiram (or renewing a prescription while searching for supply), ensure there are no concurrent medications that create major interactions:
- Warfarin: Disulfiram inhibits CYP2C9, significantly increasing warfarin levels. Monitor INR closely.
- Phenytoin: Inhibits phenytoin metabolism; monitor levels, risk of toxicity.
- Metronidazole: Contraindicated — psychotic reactions have been reported.
- Isoniazid: May cause CNS toxicity including ataxia and behavioral changes; monitor closely.
- Absolute contraindications: Severe myocardial disease, active psychosis, patient unaware of treatment.
How to Help Your Patients Find Disulfiram
For patients who specifically need disulfiram and cannot readily find it, providers can take the following steps:
- Advise the patient to search multiple pharmacies and specifically ask about 250 mg tablets (less affected than 500 mg).
- Consider rewriting the prescription as 250 mg x 2 tablets daily if the 500 mg is unavailable.
- Refer to a licensed compounding pharmacy if commercial supply is completely unavailable in the patient's area.
- — a service that calls pharmacies near the patient to find which ones have disulfiram in stock, texting results directly to the patient.
Bottom Line for Clinicians
The disulfiram shortage is a real and ongoing supply disruption that began in July 2024. As a prescriber, proactively checking availability before writing new prescriptions — and having a clear transition plan to naltrexone or acamprosate — is the best way to protect your patients' recovery. For patients already stable on disulfiram, prioritize continuity over switching unless supply is truly inaccessible.
For a practical step-by-step resource you can share with your staff, see our provider's guide to helping patients find disulfiram in stock.
Frequently Asked Questions
Yes. If a patient requires 500 mg/day and only 250 mg tablets are available, you may rewrite the prescription as two 250 mg tablets daily (with appropriate clinical judgment). This is a common workaround during the current shortage. The patient's pharmacy should be able to fill this as long as the 250 mg presentation is not also affected.
There is no required pharmacological washout from disulfiram before starting naltrexone, but you should confirm the patient has been abstinent from alcohol for at least 24-48 hours and has no active opioid use. Note that disulfiram can persist in the body for up to 14 days after the last dose — alcohol should be avoided during this period regardless of the switch.
The ASHP created the disulfiram shortage alert in July 2024 and updated it in May 2025. As of 2026, the shortage has been active for approximately 18+ months with no confirmed resolution date. Providers should assume ongoing variability in supply and plan accordingly when starting new patients on disulfiram.
Liver function tests (LFTs) should be obtained at baseline and periodically during treatment, as disulfiram can cause hepatotoxicity including fulminant hepatic failure. Patients with hepatic impairment require particular caution. Also monitor for neurological symptoms (neuropathy, psychosis) and check for drug interactions, especially warfarin (INR) and phenytoin levels.
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