Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Akorn | Location not on file | Makes it, tests it and sterilizes it | Not inspected on record |
| Akorn | Location not on file | Packages it and labels it | Not inspected on record |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, solution, concentrate
- Strength
- 100 ug per 1 mL
- Approval
- ANDA ANDA202585
- On the market since
- Nov 24, 2014
- Package NDCs
17478-055-02- Official label
- DailyMed (National Library of Medicine), updated Sep 9, 2022
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