Viatris Inc recalls Xanax XR (alprazolam) extended-release tablets, 3 mg, 60-cou
See all recalls from Viatris Inc →Recalled 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.
Hazard / Issue
Failed Dissolution Specifications: low out of specification results for dissolution.
Issued by
FDA
Distribution: Nationwide (United States)
Lot/Code Info: Lot #: DX7983, exp. date 02/28/2023
✅ What Should You Do?
- 1Stop taking this medication and contact your doctor or pharmacist immediately.
- 2Do NOT flush medications down the drain — use an FDA-approved drug take-back program.
- 3Check the lot number on your bottle or packaging against the recalled lots listed above.
- 4Report adverse events to FDA MedWatch or call 1-800-FDA-1088.
Looking for a safe alternative?
Search Amazon for Xanax XR (alprazolam) extended-release →If you were harmed by this recalled product, Top Class Actions lists active class action lawsuits and settlements that may apply to you.
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