NDC 76420-883
Hydroxyzine hydrochloride 50 mg tablet
On the label: Asclemed USA, Inc.. It's repackaged: Asclemed USA, Inc. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-502.
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
- Asclemed USA Inc. dba Enovachem, Torrance, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA204279
- On the market since
- Aug 20, 2014
- Package NDCs
76420-883-0176420-883-0576420-883-1076420-883-3076420-883-6076420-883-90- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2024
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