US Drug Recall Register
Class III · Low risk Terminated Initiated Nov 13, 2013 (13 years ago)

Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.

What was recalled

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

Recalling firm
Forest Pharmaceuticals Inc
NDC code
0456-3407-33
Origin
MO, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-1063-2014

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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