Forest Pharmaceuticals Inc recalls Namenda XR (memantine HCl), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only, F
Recalled February 12, 2014 · FDA recall D-1065-2014 · Forest Pharmaceuticals
Hazard
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing. · FDA Class III
Units
111,384 sample packs
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), sample pack, 28 mg, extended release capsules, packaged in 5-count sample packs, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045 NDC 0456-3428-05.
Manufacturer(s)
Forest Pharmaceuticals Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →