Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| ARx, LLC | Glen Rock, PA, United States | Makes it | Problems found, fixed voluntarilyJun 10, 2026 · 9 inspections |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- film, sublingual
- Strength
- 180 ug
- Approval
- NDA NDA215390
- On the market since
- Jul 1, 2022
- Package NDCs
81092-1180-081092-1180-181092-1180-3- Official label
- DailyMed (National Library of Medicine), updated Nov 25, 2025
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