NDC 0338-0719
Dextrose 70 g per 100 mL injection, solution
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Baxter Healthcare Corporation | Marion, NC, United States | Makes it, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionFeb 9, 2024 · 9 inspections, 3 with FDA action |
| Baxter Healthcare Corporation | Jayuya, PR, United States | Makes it, tests it, packages it, labels it and sterilizes it | Problems found, fixed voluntarilyJul 19, 2024 · 15 inspections, 5 with FDA action |
| Baxter Healthcare Corporation | Round Lake, IL, United States | Tests it | Serious problems, FDA actionApr 2, 2026 · 15 inspections, 2 with FDA action |
Recalls
- Dec 15, 2015 · Class I · Baxter Healthcare Corp.
Presence of Particulate Matter: Confirmed customer compliants of finding an insect floating in the primary container of each product.
Lots: Lot # C985150; Exp. 07/16
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Anhydrous Dextrose: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 70 g per 100 mL
- Approval
- NDA NDA020047
- On the market since
- Jul 2, 1991
- Package NDCs
0338-0719-06- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2019
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