Class III

Drug Recall: Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30

SUN PHARMACEUTICAL INDUSTRIES INC · June 1, 2026

Reason for Recall

Failed Impurities/Degradation Specifications

Distribution

U.S. Nationwide

States Affected

NATIONWIDE

Quantity Affected

9,048 bottles

Source: FDA (openFDA Drug Enforcement)

Recall number: D-0654-2026

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.

SUN PHARMACEUTICAL INDUSTRIES INC Drug Recall: Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30 | SafeCheck