NDC 23155-502
Hydroxyzine hydrochloride 50 mg tablet
On the label: Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc..
Where it's 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 |
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
23155-502-0123155-502-0523155-502-1023155-502-18- Official label
- DailyMed (National Library of Medicine), updated May 16, 2025
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