NDC 67046-1311
Hydroxyzine Hydrochloride 25 mg tablet, film coated
On the label: Coupler LLC. It's repackaged: Coupler LLC 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 |
Repackaging site
- Coupler LLC, West Chester, PA, United States · repackages it
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
- May 12, 2026
- Package NDCs
67046-1311-3- Official label
- DailyMed (National Library of Medicine), updated May 12, 2026
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