NDC 65219-512
Potassium Acetate 196 mg per 1 mL injection, solution, concentrate
On the label: Fresenius Kabi USA, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
Product details
- Generic drug
- Potassium Cation: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 196 mg per 1 mL
- Approval
- ANDA ANDA217515
- On the market since
- Nov 27, 2024
- Package NDCs
65219-512-0265219-512-50- Official label
- DailyMed (National Library of Medicine), updated Dec 6, 2024
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