Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alprazolam tablets Recalled by Neolpharma, Inc. Due to Subpotent Drug
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 Neolpharma, Inc. directly.
Affected Products
Alprazolam tablets, USP, CIV, 0.25 mg, Rx Only, a) 500 count bottle, b) 1000 count bottle, Distributed by: Greenstone LLC, Peapack, NJ, 07977, a) NDC 59762-3719-3, b) NDC 59762-3719-4.
Quantity: 12,310 bottles
Why Was This Recalled?
Subpotent Drug
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Neolpharma, Inc.
Neolpharma, Inc. has 1 total recall tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report