NDC 70518-4219
Dextrose 25 g per 50 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Hospira, Inc.'s NDC 0409-7517.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 25 g per 50 mL
- Approval
- NDA NDA019445
- On the market since
- Oct 23, 2024
- Package NDCs
70518-4219-070518-4219-1- Official label
- DailyMed (National Library of Medicine), updated Aug 31, 2026
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