Upsher Smith Laboratories, Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only, Ma

Recalled January 23, 2013 · FDA recall D-127-2013 · Upsher Smith Laboratories

Hazard

Labeling: Label Error On Declared Strength; Some bottles of product were missing the color-coded strength on the primary display panel of the label. · FDA Class III

Units

11,316 bottles

Sold at

Nationwide and Puerto Rico

Description

Labeling: Label Error On Declared Strength; Some bottles of product were missing the color-coded strength on the primary display panel of the label.

Product

Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valproic Acid Activity, 100-count tablets per bottle, Rx only, Manufactured by Upsher-Smith Laboratories, Inc., Minneapolis, MN 55447, NDC 0245-0182-11.

Manufacturer(s)

Upsher Smith Laboratories, Inc.

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