NDC 36000-262
Dexmedetomidine Hydrochloride 100 ug per 1 mL injection, solution, concentrate
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Pharmaceuticals India Private Limited | Ahmedabad, India | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionJan 27, 2023 · 9 inspections, 3 with FDA action |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA208103
- On the market since
- Apr 16, 2026
- Package NDCs
36000-262-0136000-262-0536000-262-1036000-262-25- Official label
- DailyMed (National Library of Medicine), updated May 29, 2026
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