drugs Class III Updated 2013-01-23

Upsher Smith Laboratories, Inc. recalls Divalproex Sodium Delayed-Release Tablets, USP, 500 mg Valpr

Recalled 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.

Hazard / Issue

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

Issued by

FDA

Distribution: Nationwide (United States)
Lot/Code Info: Lot #: 310162, Exp 09/14
View official government recall

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