US Drug Recall Register
Class II · Moderate risk Terminated Initiated Oct 11, 2018 (8 years ago)

HydrOXYzine HYDROCHLORIDE SYRUP

Class II — Moderate risk. May cause temporary or reversible harm; serious harm unlikely.

Why it was recalled

CGMP Deviations: cleaning procedures during manufacturing caused out of specification results for unknown impurities.

What was recalled

HydrOXYzine HYDROCHLORIDE SYRUP (HydrOXYzine Hydrochloride Oral Solution, USP), 10 mg per 5 mL, Rx only, Distributed by Lannett Company, Inc., Philadelphia, PA 19154, NDC 54838-502-80.

Recalling firm
Lannett Company, Inc.
NDC code
54838-502-80
Origin
PA, United States
Initiated by
Voluntary: Firm initiated
FDA recall number
D-0083-2019

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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