NDC 17271-772
Dextrose 2500 mg per 50 mL injection, solution
On the label: Becton Dickinson and Company.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 2500 mg per 50 mL
- Approval
- ANDA ANDA207449
- On the market since
- Oct 21, 2016
- Package NDCs
17271-772-0217271-772-0317271-772-05- Official label
- DailyMed (National Library of Medicine), updated Jan 8, 2026
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