NDC 70518-4170
Hydroxyzine Hydrochloride 50 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-115.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Graviti Pharmaceuticals Private Limited | Sangareddy, India | Makes it and tests it | Problems found, fixed voluntarilyJul 28, 2026 · 2 inspections |
Product details
- Generic drug
- Hydroxyzine: every company that makes it
- Form
- tablet, film coated, oral
- Strength
- 50 mg
- Approval
- ANDA ANDA217652
- On the market since
- Aug 28, 2024
- Package NDCs
70518-4170-070518-4170-170518-4170-270518-4170-370518-4170-470518-4170-570518-4170-6- Official label
- DailyMed (National Library of Medicine), updated Oct 2, 2026
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