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FDAFDA · Food and drugs·Recall number D-1092-2014

Teva Ethambutol Hydrochloride Tablets, USP, 400 mg, 100- count bottle, Rx Only,Distributed by Teva Pharmaceuticals, USA, Sellersville, PA., NDC 0555-0923-02.

Published March 12, 2014 · Recall initiated: January 24, 2014

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

CGMP Deviations: Ethambutol Hydrochloride Tablets, USP, 400 mg were manufactured using unapproved material: the incorrect gelatin excipient than specified in the product formulation.

What to do

Voluntary: Firm initiated · Letter

Recall details

Manufacturer
Teva Pharmaceuticals USA
Distributor
Nationwide.
Lot
Lot # 34013698A, Exp. 01/16. Lot # 34013699A, Exp. 01/16. Lot # 34013700A, Exp. 01/16. Lot # 34013756A, Exp. 01/16.
Risk classification
Class II
Area (FDA)
drug
Country
United States

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