Why it was recalled
cGMP Deviations
Product description
Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC 67253-901-50), and c) 1000-count bottles (NDC 67253-901-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Lot numbers, UPCs & expiration codes
Lot #: a) 19B029A, Exp. Date 02/2022; 19D021A, Exp. Date 04/2022. b) 19A087B, 19A088B, 19A089B, 19A090B, Exp. Date 02/2022; 19A086B, 19A091B, 19B019B, Exp. Date 02/2022. c) 19B020C, 19B021C, 19B027C, 19B028C, Exp. Date 02/2022, 19E056C, 19E057C, Exp. Date 05/2022; 19E059C, Exp. Date 06/2022 19G072C, Exp. Date 07/2022
Where it was sold
Nationwide within the United States
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-0565-2022
- Classification
- Class II
- Status
- Terminated
- Recall initiated
- Feb 15, 2022
- FDA report date
- Feb 23, 2022
- Quantity
- 205,662 bottles
- Recall type
- Voluntary: Firm initiated
- Recalling firm
- ANI Pharmaceuticals, Inc.
Original FDA data
Every field from FDA enforcement report D-0565-2022, exactly as published.
Show all FDA fields
- City
- Baudette
- State
- MN
- Status
- Terminated
- Country
- United States
- Event ID
- 89556
- Address
- 210 W Main St
- Code information
- Lot #: a) 19B029A, Exp. Date 02/2022; 19D021A, Exp. Date 04/2022. b) 19A087B, 19A088B, 19A089B, 19A090B, Exp. Date 02/2022; 19A086B, 19A091B, 19B019B, Exp. Date 02/2022. c) 19B020C, 19B021C, 19B027C, 19B028C, Exp. Date 02/2022, 19E056C, 19E057C, Exp. Date 05/2022; 19E059C, Exp. Date 06/2022 19G072C, Exp. Date 07/2022
- Postal code
- 56623-2467
- Report date
- Feb 23, 2022
- Product type
- Drugs
- Recall number
- D-0565-2022
- Classification
- Class II
- Recalling firm
- ANI Pharmaceuticals, Inc.
- Product quantity
- 205,662 bottles
- Termination date
- Oct 25, 2022
- Reason for recall
- cGMP Deviations
- Voluntary / mandated
- Voluntary: Firm initiated
- Product description
- Alprazolam Tablets, USP 0.5 mg, packaged in a) 100-count bottles (NDC 67253-901-10), b) 500-count bottles (NDC 67253-901-50), and c) 1000-count bottles (NDC 67253-901-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
- Distribution pattern
- Nationwide within the United States
- Recall initiation date
- Feb 15, 2022
- Initial firm notification
- Letter
- Center classification date
- Feb 17, 2022