NDC 0404-9938
Precedex 100 ug per 1 mL injection, solution, concentrate
On the label: Henry Schein, Inc.. It's repackaged: Henry Schein, Inc. rebottles it from Hospira, Inc.'s NDC 0409-1638.
Where the pills inside were 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 |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 100 ug per 1 mL
- Approval
- NDA NDA021038
- On the market since
- Jan 13, 2022
- Package NDCs
0404-9938-02- Official label
- DailyMed (National Library of Medicine), updated May 21, 2026
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