Namenda XR recall: Failed Dissolution
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.
Why was Namenda XR recalled?
Failed Dissolution Specifications: Three lots of product being recalled having failed stability dissolution testing.
What should I do if I have this product?
Review the official FDA enforcement record for current instructions.
What to do with a recalled product: refunds, receipts, safe disposal and how to report a problem.
Is my product affected?
Compare the item in your hand with every identifier below from the official FDA record. Only products that match the listed product and lot, UPC or model codes are part of this recall.
Which lot codes, UPCs or models are affected?
Lot 1112467 Exp. 02/15
- 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.
- Recalling firm
- Forest Pharmaceuticals Inc
- Quantity
- 111,384 sample packs
- Distribution
- Nationwide and Puerto Rico.
- Recall date
- February 12, 2014
- Classification
- Class III
- Status
- Terminated
- Agency
- FDA (drug)