FDA Drug recall 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…
- FDA Drug
- Class III
- terminated
- Published 2014-02-12
On 2014-02-12 the FDA classified a Class III recall of Namenda XR (memantine HCl), 7 mg extended release capsules, 30-count bottle, Rx only, Forest Pharmaceuticals Inc., St. Louis, MO 63045, NDC… by Forest Pharmaceuticals, citing failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Read the official FDA Drug notice
| Agency | FDA Drug |
|---|---|
| Recall number | D-1063-2014 |
| Classification | Class III |
| Status | terminated |
| Initiated | 2013-11-13 |
| Published | 2014-02-12 |
| Last updated | 2026-09-13 11:51 UTC |
| Company | Forest Pharmaceuticals |
| Distribution | US |
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
Reason
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
Identifiers
| code_info | Lot 1111291 Exp. 02/16 |
|---|
Status history
No status changes recorded since RecallRadar first saw this recall on 2026-09-13 11:51 UTC. Current status: terminated.
Source
Official record: https://api.fda.gov/drug/enforcement.json?search=recall_number:%22D-1063-2014%22
RecallRadar indexes public recall notices from the FDA, USDA FSIS, and CPSC. The official agency notice is the authoritative source. Always confirm details at the linked source before acting.