NDC 17271-721
Dextrose 100 mg per 1 mL injection, solution
On the label: Becton Dickinson and Company.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi Deutschland GmbH | Friedberg, Germany | Makes it, makes the active ingredient and tests it | Problems found, fixed voluntarilyDec 21, 2023 · 4 inspections |
| 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
- 100 mg per 1 mL
- Approval
- ANDA ANDA209448
- On the market since
- Feb 5, 2020
- Package NDCs
17271-721-0517271-721-0617271-721-07- Official label
- DailyMed (National Library of Medicine), updated Mar 17, 2026
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