NDC 0338-0669
Potassium Chloride in Dextrose and Sodium Chloride 5 g per 100 mL / 75 mg per 100 mL / 450 mg 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 |
Product details
- Generic drug
- Anhydrous Dextrose and Potassium Cation and Sodium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 5 g per 100 mL / 75 mg per 100 mL / 450 mg per 100 mL
- Approval
- NDA NDA018008
- On the market since
- Feb 2, 1979
- Package NDCs
0338-0669-04- Official label
- DailyMed (National Library of Medicine), updated Feb 21, 2019
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