FDAFDA · Food and drugs·Recall number D-1063-2014
Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045, NDC 0456-3407-33
Published February 12, 2014 · Recall initiated: November 13, 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
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
What to do
Voluntary: Firm initiated · Letter
Recall details
- Manufacturer
- Forest Pharmaceuticals Inc
- Distributor
- Nationwide and Puerto Rico.
- Lot
- Lot 1111291 Exp. 02/16
- Risk classification
- Class III
- Area (FDA)
- drug
- Country
- United States
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