NDC 70518-1692

Hydroxyzine hydrochloride 25 mg tablet

On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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, oral
Strength
25 mg
Approval
ANDA ANDA204279
On the market since
Nov 26, 2018
Package NDCs
70518-1692-0 70518-1692-1 70518-1692-2
Official label
DailyMed (National Library of Medicine), updated Jul 10, 2026

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