Viatris Inc recalls alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 079
Recalled May 11, 2022 · FDA recall D-0844-2022 · Viatris
Hazard
Failed Dissolution Specifications: low out-of-specification dissolution test results observed. · FDA Class II
Units
6,789 bottles
Sold at
Product was distributed nationwide in the USA
Description
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Product
alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.
Manufacturer(s)
Viatris Inc
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →