Qualitest Pharmaceuticals recalls Disulfiram tablets, USP, 500 mg, 100-count bottles, Rx only, Manufactured for and by Qualitest Pharmaceuticals 130 Vinta

Recalled July 8, 2015 · FDA recall D1151-2015 · Qualitest Pharmaceuticals

Hazard

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. · FDA Class III

Units

2016 bottles

Sold at

Nationwide

Description

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.

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.

Manufacturer(s)

Qualitest Pharmaceuticals

Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →