NDC 71335-2451

Hydroxyzine Hydrochloride 25 mg tablet, film coated

On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from KVK-TECH, Inc.'s NDC 10702-011.

United States: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
Kvk-Tech, Inc.Newtown, PA, United StatesMakes it Serious problems, FDA actionMar 14, 2025 · 13 inspections, 3 with FDA action

Repackaging site

Recalls

Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.

Product details

Generic drug
Hydroxyzine: every company that makes it
Form
tablet, film coated, oral
Strength
25 mg
Approval
ANDA ANDA040786
On the market since
Jul 24, 2012
Package NDCs
71335-2451-1 71335-2451-2 71335-2451-3 71335-2451-4 71335-2451-5 71335-2451-6 71335-2451-7 71335-2451-8
Official label
DailyMed (National Library of Medicine), updated Aug 20, 2024

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