NDC 51662-1649
Hydroxyzine Hydrochloride 25 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from American Regent, Inc.'s NDC 0517-4201.
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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- injection, solution, intramuscular
- Strength
- 25 mg per 1 mL
- Approval
- ANDA ANDA087408
- On the market since
- Sep 30, 1990
- Package NDCs
51662-1649-251662-1649-3- Official label
- DailyMed (National Library of Medicine), updated May 28, 2024
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