NDC 0781-3495
Dexmedetomidine Hydrochloride In 0.9% Sodium Chloride 4 ug per 1 mL injection
On the label: Sandoz Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Jiangsu Hengrui Pharmaceuticals Co., Ltd. (Dongjin Road Site) | Lianyungang, China | Makes it | Problems found, fixed voluntarilyAug 29, 2023 · 2 inspections |
Product details
- Generic drug
- Dexmedetomidine: every company that makes it
- Form
- injection, intravenous
- Strength
- 4 ug per 1 mL
- Approval
- ANDA ANDA209065
- On the market since
- Jun 12, 2020
- Package NDCs
0781-3495-95- Official label
- DailyMed (National Library of Medicine), updated Sep 8, 2026
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