Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
alprazolam XR extended-release tablets Recalled by Viatris Inc Due to Failed Dissolution Specifications: low out-of-specification dissolution test results...
What You Should Do
Stop using this product immediately. Do not consume, use, or distribute it.
Return the product to the place of purchase for a full refund. If you have questions, contact Viatris Inc directly.
Affected Products
alprazolam XR extended-release tablets, 3 mg, 60-count bottle, Rx only, Distributed by: Greenstone LLC, Peapack, NJ 07977, NDC 59762-0068-1.
Quantity: 6,789 bottles
Why Was This Recalled?
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Viatris Inc
Viatris Inc has 22 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report