FDAFDA · Food and drugs·Recall number D-331-2013
Glenmark Topiramate Tablets, 200 mg, 60-count bottle, (NDC 68462-110-60), Rx only, Manufactured by Glenmark Generics Ltd.Colvale- Bardez Ltd 403513, India Manufactured for : Glenmark Generics USA Mahwah, NJ 07430
Published May 22, 2013 · Recall initiated: April 5, 2013
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
Chemical Contamination: Topiramate Tablets is being recalled due to complaints related to an off - odor. described as moldy, musty or fishy in nature.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Brand
- TOPIRAMATE
- Manufacturer
- Glenmark Generics Inc., USA
- Distributor
- Nationwide
- UPC
- 0368462109601
- Lot
- Lot# 02123782, Exp 11/14
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
Sell products like this?
Recalert watches your whole catalog for recalls like this one, automatically.