United StatesXanax XR (alprazolam) extended‑release tablets, 3 mg, in 60‑tablet prescription bottles (NDC 58151-506-91), lot 8177156, exp 02/28/2027, distributed by Viatris Specialty LLC (Morgantown, WV) and made in Ireland, is affected. Viatris, Inc. is recalling this lot nationwide in the United States because it failed dissolution specifications.
What's being recalled
Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91
Recalling firm: Viatris, Inc., Canonsburg, PA, United States.
How to identify it
Lot# 8177156, Exp Date: 02/28/2027
The hazard
Failed Dissolution Specifications
What to do
Don't stop taking a prescribed medicine without talking to your doctor or pharmacist first. For other products, stop using them and ask the pharmacist, seller or maker what to do.
The notice doesn't give instructions for consumers, so this is general advice for health & beauty recalls. Check the official notice for the details.
Where it was sold
US Nationwide.
The official notice
This page is a summary of the notice published by U.S. Food and Drug Administration (enforcement reports), collected from U.S. Food and Drug Administration (enforcement reports). Check the original before you act on it.
Read the official notice (opens in a new tab)