Viat: Viatris recalls 3mg alprazolam XR tablets due to failed dissolution testing. This may affect medication effectiveness. Check NDC 59762-0068-1 and lot # EH834: 07977, exp. August 2023.
Failed Dissolution Specifications: low out-of-specification dissolution test results observed.
Viatris has recalled 3mg alprazolam XR extended-release tablets (60-count bottles) because they failed dissolution tests. This could mean the medication doesn't work as intended, so affected users should stop using the product and contact their doctor.
The tablets failed dissolution tests, meaning they may not release the medication properly in the body. This could lead to inconsistent dosing or reduced effectiveness, but it does not cause immediate harm or injury.
People with prescriptions for alprazolam XR 3mg tablets who received this specific bottle from Greenstone LLC in Peapack, NJ. Those with the NDC 59762-0068-1 and lot # EH8348 are most at risk.
Look for the product name 'alprazolam XR extended-release tablets, 3 mg, 60-count bottle' with NDC 59762-0068-1 and lot number EH8348. The expiration date is August 2023.
Verify the NDC code 59762-0068-1 and lot number EH8348 on the bottle label.
Talk to your healthcare provider about alternative medications if you have the recalled product.
The recall indicates the product failed dissolution tests, which may affect effectiveness but does not cause immediate harm. Consult your doctor for advice.
Check for NDC 59762-0068-1 and lot number EH8348 on the bottle label. The expiration date is August 2023.
Contact your doctor to discuss alternatives. The recall does not require immediate disposal but may need replacement.
We’ve drafted a message you can send Viatris to request your refund or repair — edit it as you like.
Subject: Recall D-0844-2022 — Viatris Viatris Hello, I own a Viatris that is covered by recall D-0844-2022 from Viatris. I’m writing to arrange the remedy described in the recall (a refund, repair, or replacement as applicable). Could you please tell me the next steps to resolve this? Thank you.
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The facts (hazard, remedy, dates, manufacturer) are pulled from the official FDA recall record. The plain-language summary and step-by-step checklist are written by GovInfoNow to make the official notice easier to act on — they don’t replace it.
