NDC 65219-150
Potassium Chloride in Dextrose and Sodium Chloride 25 g per 500 mL / 2.25 g per 500 mL / 0.745 g per 500 mL injection, solution
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| 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 and Potassium Cation and Sodium Cation: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 25 g per 500 mL / 2.25 g per 500 mL / 0.745 g per 500 mL
- Approval
- ANDA ANDA213523
- On the market since
- Aug 26, 2022
- Package NDCs
65219-150-0065219-150-75- Official label
- DailyMed (National Library of Medicine), updated May 6, 2024
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