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

Recall Number: D-0654-2026

Firm: SUN PHARMACEUTICAL INDUSTRIES INC

Classification: Class III

Status: Ongoing

Report Date: 20260708

Initiation Date: 20260601

Termination Date:

Reason for Recall

Failed Impurities/Degradation Specifications

Product Description

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

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Data source: openFDA · Updated regularly