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FDAFDA · Food and drugs·Recall number D-0833-2020

Lamotrigine Tablets, USP, 100 mg, Rx Only, 100-count bottle, Mfd. by: Taro Pharmaceutical Industries Ltd. Haifa Bay, Israel 2624761 Dist. by: Taro Pharmaceuticals U.S.A., Inc. Hawthorne, NY 10532, NDC 51672-4131-1.

Published February 19, 2020 · Recall initiated: December 20, 2019

Status when published: Terminated — openFDA updates weekly, so this field may not reflect the current status. Always confirm with the official notice.

What's the hazard

Cross Contamination; Lamotrigine Tablets 100 mg USP was contaminated with enalapril maleate.

What to do

Voluntary: Firm initiated · Letter

Recall details

Brand
LAMOTRIGINE
Manufacturer
Taro Pharmaceuticals U.S.A., Inc.
Distributor
Nationwide in the U.S. and Puerto Rico.
UPC
0351672413019
Lot
Lot #: 331771, Exp. June 2021
Risk classification
Class I
Area (FDA)
drug
Country
United States

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