NDC 60687-875
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: American Health Packaging. It's repackaged: American Health Packaging rebottles it from Aurobindo Pharma Limited's NDC 59651-501.
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
- American Health Packaging, Columbus, OH, United States · repackages it
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA087871
- On the market since
- Sep 11, 2025
- Package NDCs
60687-875-0160687-875-11- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2025
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