NDC 70518-4141
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Rising Pharma Holdings, Inc.'s NDC 16571-114.
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
- 25 mg
- Approval
- ANDA ANDA217652
- On the market since
- Jul 16, 2024
- Package NDCs
70518-4141-070518-4141-170518-4141-2- Official label
- DailyMed (National Library of Medicine), updated Aug 27, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?