Class II

Drug Recall: Sertraline Hydrochloride Tablets USP, 100 mg, 90 Tablets bottles, Rx Only, Manufactured by: Lupin Pharmaceuticals, Inc., Naples, FL 34108, NDC 68180-353-09.

Lupin Pharmaceuticals Inc. · November 5, 2025

Reason for Recall

Defective container - seal not adhering to bottles

Distribution

Nationwide.

States Affected

NATIONWIDE

Quantity Affected

52,128 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0227-2026

Status: ongoing

SafeCheck provides drug interaction information from FDA-approved product labeling (openFDA). This is for informational purposes only and is not medical advice. Always consult your healthcare provider before making medication decisions.