NDC 70934-655
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Denton Pharma, Inc. DBA Northwind Pharmaceuticals.. It's repackaged: Denton Pharma, Inc. DBA Northwind Pharmaceuticals. rebottles it from Epic Pharma, LLC's NDC 42806-160.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Epic Pharma, LLC | Laurelton, NY, United States | Makes it | Problems found, fixed voluntarilyJun 12, 2026 · 14 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, film coated
- Strength
- 25 mg
- Approval
- ANDA ANDA040602
- On the market since
- Apr 1, 2020
- Package NDCs
70934-655-2070934-655-30- Official label
- DailyMed (National Library of Medicine), updated Jul 15, 2020
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