NDC 33261-161

Hydroxyzine hydrochloride 25 mg tablet

On the label: Aidarex Pharmaceuticals LLC. It's repackaged: Aidarex Pharmaceuticals LLC rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-501.

United States: 2India: 1

Where the pills inside were made

FactoryWhereRoleLast FDA inspection
CorePharma, LLCMiddlesex, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundAug 28, 2025 · 14 inspections, 3 with FDA action
Emcure Pharmaceuticals LimitedSurendranagar, IndiaMakes it, tests it, packages it and labels it No problems foundOct 10, 2025 · 1 inspection
Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.East Brunswick, NJ, United StatesMakes it, tests it, packages it and labels it No problems foundSep 19, 2023 · 10 inspections

Product details

Generic drug
Hydroxyzine: every company that makes it
Form
tablet
Strength
25 mg
Approval
ANDA ANDA204279
On the market since
Mar 24, 2012
Package NDCs
33261-161-15 33261-161-20 33261-161-30 33261-161-40 33261-161-60 33261-161-90
Official label
DailyMed (National Library of Medicine), updated Mar 9, 2017

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