Disulfiram tablets — Class III drug recall D1151-2015
Terminated recall by Qualitest Pharmaceuticals, reported 2015-07-08, distributed nationwide. Failed Dissolution Specifications: During routine stability testing at the 12 month time point, one product lo
| Recall number | D1151-2015 |
|---|---|
| Product type | Drug |
| Classification | Class III |
| Status | Terminated |
| Voluntary or mandated | Voluntary |
| Recalling firm | Qualitest Pharmaceuticals, Huntsville, AL, United States |
| Recall initiated | 2015-06-18 |
| Classified | 2015-06-30 |
| Reported by FDA | 2015-07-08 |
| Terminated | 2016-10-23 |
| Distributed | Nationwide (US) |
| Quantity | 2,016 bottles |
| Reason classes | specification failure |
| NDC | 00603-3432-21 |
| Lot numbers | 01/16, T142A14A, T143A14A, T144A14A |
Product
Disulfiram tablets, USP, 500 mg, 100-count bottles, Rx only, Manufactured for and by Qualitest Pharmaceuticals 130 Vintage Drive Huntsville, AL 35811. NDC 0603-3432-21.
Reason for recall
Failed Dissolution Specifications: During routine stability testing at the 12 month time point, one product lot was found to be out of specification for dissolution.
Machine access
This record, with every extracted code, the verbatim FDA record and provenance, is available from the recall API: GET https://api.data.aroqon.com/v1/recalls/D1151-2015. Look up any UPC, UDI, NDC or lot with /v1/recalls/lookup?code=…. API docs · free and paid keys.
Source: U.S. Food and Drug Administration enforcement report via openFDA (CC0). Structured by Data Foundry (recall-structuring@2); last changed 2026-09-26. Not affiliated with or endorsed by FDA. Not medical or legal advice.