US Drug Recall Register
Class III · Low risk Terminated Initiated Dec 13, 2019 (7 years ago)

Memantine Hydrochloride Extended-release Capsules, 28mg, packaged in 100-count Unit Dose…

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

Why it was recalled

Failed Dissolution Specifications: High out of specification result observed at stability studies.

What was recalled

Memantine Hydrochloride Extended-release Capsules, 28mg, packaged in 100-count Unit Dose Cartons , Rx only, Manufactured for: Lupin Pharmaceuticals, Inc., Baltimore, Maryland 21202 United States; Distributed by: Major Pharmaceuticals, 17177 N Laurel Park Dr., Suite 233, Livonia, MI 48152 USA, NDC 0904-6735-61

Recalling firm
The Harvard Drug Group
NDC code
0904-6735-61
Origin
MI, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0844-2020

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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