Potential health hazard — use of or exposure to this product may cause temporary or medically reversible adverse health consequences.
Nadolol Tablets Recalled by Sandoz Incorporated Due to Failed dissolution specification: recalled due to an out...
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 Sandoz Incorporated directly.
Affected Products
Nadolol Tablets, USP, 40mg, packaged in 1000-count bottle, Rx Only, Manufactured by Sandoz Inc., Princeton, NJ 08540, NDC 0781-1182-10
Quantity: 96 bottles
Why Was This Recalled?
Failed dissolution specification: recalled due to an out of specification dissolution result of 40% (Specification: NLT 80%)
Where Was This Sold?
This product was distributed to 2 states: MS, OH
About Sandoz Incorporated
Sandoz Incorporated has 16 total recalls tracked by RecallDetector.
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Data sourced from the FDA (Drug). Last updated March 26, 2026. View original report