Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Lannett Ranitidine Syrup (Ranitidine Oral Solution Recalled by Lannett Company, Inc. Due to CGMP Deviations: Presence of NDMA impurity detected in...
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 Lannett Company, Inc. directly.
Affected Products
Lannett Ranitidine Syrup (Ranitidine Oral Solution, USP), 15mg/mL Rx Only Distributed by: Lannett Company, Inc. Philadelphia, PA 19154 NDC 54838-550-80
Quantity: 683,149 bottles
Why Was This Recalled?
CGMP Deviations: Presence of NDMA impurity detected in product.
Where Was This Sold?
This product was distributed nationwide across all 50 states.
About Lannett Company, Inc.
Lannett Company, Inc. has 5 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report