NDC 24658-783

Hydroxyzine Hydrochloride 50 mg tablet, film coated

On the label: PuraCap Laboratories LLC dba Blu Pharmaceuticals.

United States: 1

Where it's made

FactoryWhereRoleLast FDA inspection
Epic Pharma, LLCLaurelton, NY, United StatesMakes it Problems found, fixed voluntarilyJun 12, 2026 · 14 inspections

Product details

Generic drug
Hydroxyzine: every company that makes it
Form
tablet, film coated, oral
Strength
50 mg
Approval
ANDA ANDA040604
On the market since
Jul 21, 2021
Package NDCs
24658-783-10
Official label
DailyMed (National Library of Medicine), updated Feb 2, 2026

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