Forest Pharmaceuticals Inc recalls Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St. L
Recalled February 12, 2014 · FDA recall D-1063-2014 · Forest Pharmaceuticals
Hazard
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing. · FDA Class III
Units
156 bottles
Sold at
Nationwide and Puerto Rico.
Description
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Product
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
Manufacturer(s)
Forest Pharmaceuticals Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →