NDC 50436-0501

Hydroxyzine hydrochloride 25 mg tablet

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

Where the pills inside were made

CorePharma, LLC

Middlesex, NJ, United States · makes it, tests it, packages it and labels it

No problems found Last FDA inspection Aug 28, 2025. 14 inspections on record, 3 with serious problems.

Emcure Pharmaceuticals Limited

Surendranagar, India · makes it, tests it, packages it and labels it

No problems found Last FDA inspection Oct 10, 2025. 1 inspection on record.

Repackaging site

Product details

Generic drug
Hydroxyzine: see every company that makes it
Form
tablet
Strength
25 mg
Approval
ANDA ANDA204279
On the market since
Mar 24, 2012
Package NDCs
50436-0501-1
Official label
DailyMed (National Library of Medicine), updated Feb 12, 2019

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