NDC 43066-557
Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride 400 ug per 100 mL injection
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Healthcare Corporation | Round Lake, IL, United States | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionApr 2, 2026 · 15 inspections, 2 with FDA action |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, intravenous
- Strength
- 400 ug per 100 mL
- Approval
- ANDA ANDA208532
- On the market since
- Aug 27, 2019
- Package NDCs
43066-557-12- Official label
- DailyMed (National Library of Medicine), updated Sep 24, 2026
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