RecallDepth
Class III Terminated

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.

Company
Upsher Smith Laboratories, Inc.
Recall Initiated
December 10, 2012
Posted
January 23, 2013
Recall Number
D-127-2013
Voluntary / Mandated
Voluntary: Firm initiated
Quantity
11,316 bottles
Firm Location
Maple Grove, MN, United States

Reason for Recall

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

Distribution

Nationwide and Puerto Rico

Lot / Code Info

Lot #: 310162, Exp 09/14

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