NDC 65219-238
Dextrose 12500 mg per 250 mL injection, solution
On the label: Fresenius Kabi USA, LLC.
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
- 12500 mg per 250 mL
- Approval
- ANDA ANDA207449
- On the market since
- Oct 21, 2016
- Package NDCs
65219-238-0165219-238-25- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2025
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