SUN PHARMACEUTICAL INDUSTRIES INC recalls Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories,
Recalled July 8, 2026 · FDA recall D-0654-2026 · SUN PHARMACEUTICAL INDUSTRIES
Hazard
Failed Impurities/Degradation Specifications · FDA Class III
Units
9,048 bottles
Sold at
U.S. Nationwide
Description
Failed Impurities/Degradation Specifications
Product
Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle, Distributed by: Ohm Laboratories, Inc., New Brunswick, NJ 08901. NDC 66336-561-30
Manufacturer(s)
SUN PHARMACEUTICAL INDUSTRIES INC
Source: U.S. Food and Drug Administration. Official recall notice on fda.gov →