NDC 55150-296
Dexmedetomidine Hydrochloride 4 ug per 1 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 4 ug per 1 mL
- Approval
- ANDA ANDA210321
- On the market since
- Dec 7, 2020
- Package NDCs
55150-296-10- Official label
- DailyMed (National Library of Medicine), updated Jul 20, 2026
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?