NDC 59651-501
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: Aurobindo Pharma Limited.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Apl Healthcare Limited | Mahabubnagar, India | Makes it and tests it | No problems foundJan 18, 2023 · 2 inspections |
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
- Oct 7, 2021
- Package NDCs
59651-501-0159651-501-0559651-501-99- Official label
- DailyMed (National Library of Medicine), updated Mar 3, 2026
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