Dr. Reddy's Laboratories, Inc.: IBU Ibuprofen Tablets, USP, 800 mg
Recall reason: Failed impurities/degradation specifications: results for unknown impurity, were 0.13% and 0.11% respectively, exceeding the 0.10% specification limit.. Recalled by Dr. Reddy's Laboratories, Inc.. Distribution: Nationwide in the USA and Puerto Rico. Classification (Class II — potential health risk). Affected lots/NDC/dates: a) NDC 55111-684-01 Lots C2207525, Exp 5/31/2026; C2212902, Exp 11/30/2026. b) NDC 55111-684-05 Lots C2207526, Exp 5/3. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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