NDC 53002-3901
Hydroxyzine hydrochloride 10 mg tablet
On the label: RPK Pharmaceuticals, Inc.. It's repackaged: RPK Pharmaceuticals, Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-500.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| CorePharma, LLC | Middlesex, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundAug 28, 2025 · 14 inspections, 3 with FDA action |
| Emcure Pharmaceuticals Limited | Surendranagar, India | Makes 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 States | Makes it, tests it, packages it and labels it | No problems foundSep 19, 2023 · 10 inspections |
Repackaging site
- RPK Pharmaceuticals, Inc., Union City, California, United States · repackages it and relabels it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet
- Strength
- 10 mg
- Approval
- ANDA ANDA204279
- On the market since
- Aug 20, 2014
- Package NDCs
53002-3901-153002-3901-253002-3901-3- Official label
- DailyMed (National Library of Medicine), updated Dec 21, 2020
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