Recall
FDAHealthMarch 17, 2026

Viatris, Inc. — 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

⚠️ Failed Dissolution Specifications

Is this relevant to me?

Geography
Nationwide
Source agency
FDA
Category
Health
Published
March 17, 2026

US Nationwide.

What's affected?

Product
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
Brand
XANAX
UPC
0358151506910
Lot code
8177156

Additional details

Lot# 8177156, Exp Date: 02/28/2027

What should I do?

Recommended action

Class II recall. Voluntary: Firm initiated

View original FDA notice →

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