# FDA recall D1151-2015

> **Qualitest Pharmaceuticals** · Class III · drug recall initiated 2015-06-18.

## 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.

## Distribution

Nationwide

## Key facts

- **Recall number:** D1151-2015
- **Recalling firm:** Qualitest Pharmaceuticals
- **Classification:** Class III
- **Product type:** drug
- **Status:** Terminated
- **Initiation date:** 2015-06-18
- **Report date:** 2015-07-08
- **Termination date:** 2016-10-23

- **Voluntary/Mandated:** Voluntary: Firm initiated
- **Location:** Huntsville, AL, United States

## Primary source

FDA Enforcement Reports: https://www.accessdata.fda.gov/scripts/ires/index.cfm?Product=D1151-2015

## Citation

> AI Analytics. FDA recall D1151-2015. Retrieved 2026-05-26 from https://api.ai-analytics.org/recall/D1151-2015. Source: US FDA. Licensed CC0.

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