Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Di
Recalled May 18, 2022 · FDA recall D-0854-2022 · Viatris
Hazard
Failed Dissolution Specifications: low out of specification results for dissolution. · FDA Class II
Units
110 bottles
Sold at
Product was distributed nationwide in the USA
Description
Failed Dissolution Specifications: low out of specification results for dissolution.
Product
Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by Pharmacia & Upjohn Co, Division of Fizer Inc, NY, NY 10017, NDC 0009-0068-07.
Manufacturer(s)
Viatris Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →