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Fexofenadine Hydrochloride Tablets recall

SUN PHARMACEUTICAL INDUSTRIES INC recalled Fexofenadine Hydrochloride Tablets on July 8, 2026 because of failed Impurities/Degradation Specifications. It was sold nationwide.

Why it was recalled

Failed Impurities/Degradation Specifications

What's 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

Quantity: 9,048 bottles

What to do

Check whether you have the product (match the lot numbers, dates or codes in the official notice). Stop using it, and return it or throw it away as the notice says.

Read the official FDA notice

Details

Company
SUN PHARMACEUTICAL INDUSTRIES INC, Princeton, NJ
Date
Severity
Class III
the product is unlikely to cause health problems but breaks a rule.
Where sold
Nationwide
U.S. Nationwide
Status
Ongoing
Recall number
D-0654-2026
Source
U.S. Food and Drug Administration

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