Why it was recalled
Failed Dissolution Specifications
Product description
Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91
Lot numbers, UPCs & expiration codes
Lot# 8177156, Exp Date: 02/28/2027
Where it was sold
US Nationwide.
What to do if you have this product
- Compare the lot number and expiration date on your package with the codes above.
- Don't stop taking a prescription medicine on your own. Call your pharmacist or doctor; they can confirm whether your supply is affected and arrange a replacement.
- If you have symptoms you think are related, contact your doctor. In an emergency call 911.
- Report side effects to FDA MedWatch at 1-800-FDA-1088.
Recall details
- Recall number
- D-0444-2026
- Classification
- Class II
- Status
- Ongoing
- Recall initiated
- Mar 17, 2026
- FDA report date
- Apr 15, 2026
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- Viatris, Inc.
Original FDA data
Every field from FDA enforcement report D-0444-2026, exactly as published.
Show all FDA fields
- City
- Canonsburg
- State
- PA
- Status
- Ongoing
- Country
- United States
- Event ID
- 98613
- Address
- 1000 Mylan Blvd
- Code information
- Lot# 8177156, Exp Date: 02/28/2027
- Postal code
- 15317-5853
- Report date
- Apr 15, 2026
- Product type
- Drugs
- Recall number
- D-0444-2026
- Classification
- Class II
- Recalling firm
- Viatris, Inc.
- Reason for recall
- Failed Dissolution Specifications
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Xanax XR, alprazolam, extended-release tablets, 3 mg, 60 Tablets bottles, Rx only, Distributed by: Viatris Specialty LLC, Morgantown, WV 06506, U.S.A, Made in Ireland, NDC 58151-506-91
- Distribution pattern
- US Nationwide.
- Recall initiation date
- Mar 17, 2026
- Initial firm notification
- Letter
- Center classification date
- Apr 8, 2026