NDC 71335-3035
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack rebottles it from Aurobindo Pharma Limited's NDC 59651-500.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
Repackaging site
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 25 mg
- Approval
- ANDA ANDA087871
- On the market since
- Oct 7, 2021
- Package NDCs
71335-3035-1- Official label
- DailyMed (National Library of Medicine), updated Jun 22, 2026
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