NDC 70934-150
Hydroxyzine hydrochloride 25 mg tablet
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Heritage Pharmaceuticals Inc. d/b/a Avet Pharmaceuticals Inc.'s NDC 23155-501.
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
- Denton Pharma, Inc. DBA Northwind Pharmaceuticals, Location not on file · repackages it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet
- Strength
- 25 mg
- Approval
- ANDA ANDA204279
- On the market since
- Aug 15, 2018
- Package NDCs
70934-150-30- Official label
- DailyMed (National Library of Medicine), updated Jan 14, 2021
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