Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals recalls HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHA

Recalled November 28, 2012 · FDA recall D-057-2013 · Vintage Pharmaceuticals LLC

Hazard

Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components. · FDA Class I

Units

14,445 bottles

Sold at

Nationwide.

Description

Superpotent (Multiple Ingredient) Drug: Confirmed customer complaints of oversized tablets resulting in superpotent assays of both the hydrocodone and acetaminophen components.

Product

HYDROCODONE BITARTRATE and ACETAMINOPHEN TABLETS, USP, 10 mg/500 mg, 100-count bottle, Rx only, Mfg. for: QUALITEST PHARMACEUTICALS, HUNTSVILLE, AL 35811, NDC 0603-3888-21

Manufacturer(s)

Vintage Pharmaceuticals LLC DBA Qualitest Pharmaceuticals

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