Viatris recalls Xanax XR alprazolam extended-release tablets 3 mg over failed dissolution specifications
The notice says Xanax XR (alprazolam) extended-release tablets, 3 mg, in 60 Tablets bottles failed dissolution specifications, and it was sent to customers across the US.
What to do
The notice does not give instructions. Read the official notice for details.
Note from Recalled Today: Don't stop taking a prescribed medicine before you talk to your pharmacist or doctor.
Recall details
- 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
- Company
- Viatris, Inc.
- Hazard
- Failed Dissolution Specifications
- Where sold
- US Nationwide.
- FDA classification
- Class II · Ongoing
- Classified by FDA
- April 8, 2026
- Recall started
- March 17, 2026
- FDA enforcement report
- April 15, 2026
- Identifiers
- Codes: Lot# 8177156, Exp Date: 02/28/2027
- FDA recall number: D-0444-2026
The headline, summary and steps above are written in plain English from the official notice below. Identifiers are copied exactly as the agency published them. Always check the official notice before you act.
Official notice
The notice's own wording from FDA.
- 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
- Reason for recall
- Failed Dissolution Specifications
- Classification
- Class II (Ongoing)
- Distribution
- US Nationwide.
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