NDC 65219-236
Dextrose 5000 mg per 100 mL injection, solution
On the label: Fresenius Kabi USA, LLC.
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 |
| HP Halden Pharma AS | Halden, Norway | Makes it, tests it and packages it | Problems found, fixed voluntarilyMay 10, 2023 · 7 inspections |
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 5000 mg per 100 mL
- Approval
- ANDA ANDA207449
- On the market since
- Oct 21, 2016
- Package NDCs
65219-236-0165219-236-10- Official label
- DailyMed (National Library of Medicine), updated Dec 17, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?