US Drug Recall Register
Class III · Low risk Ongoing Initiated Jun 1, 2026 (3 months ago)

Fexofenadine Hydrochloride Tablets, USP 180 mg, Antihistamine, 150 Tablets per bottle…

Class III — Low risk. Unlikely to cause harm, but violates FDA regulations.

Why it was recalled

Failed Impurities/Degradation Specifications

What was recalled

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

Recalling firm
Sun Pharmaceutical Industries INC
NDC code
66336-561-30
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0654-2026

What should you do? A recall doesn't always mean your specific bottle is affected - it often applies to certain lots only. Check the lot number on your package against the FDA notice, and talk to your pharmacist before stopping any medication.

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