NDC 67046-279
Hydroxyzine hydrochloride 50 mg tablet
On the label: Coupler Enterprises Inc.. It's repackaged: Coupler Enterprises 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
- Coupler Enterprises, Location not on file · repackages it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet
- Strength
- 50 mg
- Approval
- ANDA ANDA204279
- On the market since
- Oct 2, 2017
- Package NDCs
67046-279-0767046-279-1467046-279-1567046-279-2067046-279-2167046-279-2867046-279-3067046-279-60- Official label
- DailyMed (National Library of Medicine), updated Oct 2, 2017
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