Apotex Corp.: Paroxetine Hydrochloride Tablets USP
Recall reason: Failed Impurities/Degradation Specifications-Out of specification (OOS) results for the excipient Amadori Glucose adduct of Paroxetine. Recalled by Apotex Corp.. Distribution: Nationwide. Classification (Class II — potential health risk). Affected lots/NDC/dates: Lot numbers: a)100 count bottle: RV2376, RV2377; b) 1000 count bottle: RV2379, RV2380; c) 30 count bottle: RV2375; Exp.. Return the recalled medication to the pharmacy where you purchased it for a full refund of the purchase price.
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