US Drug Recall Register
Class III · Low risk Terminated Initiated Apr 18, 2017 (9 years ago)

Children's Cetirizine Hydrochloride Chewable Tablets

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

Why it was recalled

Failed Tablet/Capsule Specifications: out of specification results for increased tablet hardness.

What was recalled

Children's Cetirizine Hydrochloride Chewable Tablets, 5 mg, 30-count bottle, Manufactured by: Sun Pharmaceutical Ind. Ltd., Halol-Baroda Highway, Halol - 389 350, Gujarat, India; Distributed by: Sun Pharmaceutical Industries, Inc., Cranbury, NJ 08512, NDC 47335-343-83.

Recalling firm
Sun Pharmaceutical Industries, Inc.
NDC code
47335-343-83
Origin
NJ, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0857-2017

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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