Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alprazolam Tablets Recalled by ANI Pharmaceuticals, Inc. Due to cGMP Deviations
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 ANI Pharmaceuticals, Inc. directly.
Affected Products
Alprazolam Tablets, USP 0.25 mg, packaged in a) 100-count bottles (NDC 67253-900-10), b) 500-count bottles (NDC 67253-900-50), and c) 1000-count bottles (NDC 67253-900-11), Rx only, Distributed by: Par Pharmaceutical Chestnut Ridge, NY 10977
Quantity: 73,920 bottles
Why Was This Recalled?
cGMP Deviations
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About ANI Pharmaceuticals, Inc.
ANI Pharmaceuticals, Inc. has 11 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report