Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Alprazolam Tablets Recalled by Breckenridge Pharmaceutical, Inc Due to CGMP Deviations: Potential risk of Cross Contamination
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 Breckenridge Pharmaceutical, Inc directly.
Affected Products
Alprazolam Tablets, USP, 2 mg, CIV, packaged in: a)100-count bottle (NDC 51991-0707-01) and b) 500-count bottle (NDC 51991-0707-05), Rx only, Manufactured by Centaur Pharmaceuticals PVT. LTD., Hinjewadi, Pune, INDIA, Distributed by: Breckenridge Pharmaceuticals, Inc., Berlin, CT 06037.
Quantity: N/A
Why Was This Recalled?
CGMP Deviations: Potential risk of Cross Contamination
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Breckenridge Pharmaceutical, Inc
Breckenridge Pharmaceutical, Inc has 20 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report