Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
| Pfizer Healthcare India Private Limited | Anakapalli, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 4 ug per 1 mL
- Approval
- NDA NDA021038
- On the market since
- Apr 8, 2013
- Package NDCs
0409-1660-100409-1660-200409-1660-220409-1660-350409-1660-500409-1660-55- Official label
- DailyMed (National Library of Medicine), updated May 20, 2026
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