NDC 0404-9878
Hydroxyzine 50 mg per 1 mL injection, solution
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from American Regent, Inc.'s NDC 0517-5602.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| American Regent, Inc. | Shirley, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyApr 24, 2024 · 12 inspections, 1 with FDA action |
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- injection, solution, intramuscular
- Strength
- 50 mg per 1 mL
- Approval
- ANDA ANDA087408
- On the market since
- Jan 17, 2022
- Package NDCs
0404-9878-02- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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