NDC 0338-0143
Dextrose and Electrolyte No. 48 6 ingredients injection
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, makes the active ingredient, tests it, packages it, labels it and sterilizes it | Serious problems, FDA actionFeb 9, 2024 · 9 inspections, 3 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 |
Product details
- Generic drug
- Sodium Lactate, Potassium Chloride, Magnesium Chloride, Monobasic Potassium Phos: every company that makes it
- Form
- injection, intravenous
- Strength
- 6 ingredients
- Approval
- NDA NDA017484
- On the market since
- Feb 2, 1979
- Package NDCs
0338-0143-03- Official label
- DailyMed (National Library of Medicine), updated Feb 13, 2020
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