NDC 70121-1712
Dexmedetomidine Hydrochloride 4 ug per 1 mL injection
On the label: Amneal Pharmaceuticals LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals Private Limited | Mehsana, India | Makes it, tests it, packages it, labels it and sterilizes it | Not inspected on record |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, intravenous
- Strength
- 4 ug per 1 mL
- Approval
- ANDA ANDA216604
- On the market since
- May 19, 2023
- Package NDCs
70121-1712-270121-1712-3- Official label
- DailyMed (National Library of Medicine), updated May 19, 2026
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