NDC 51754-2001
Potassium Acetate 3.93 g per 20 mL injection, solution, concentrate
On the label: Exela Pharma Sciences, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Exela Pharma Sciences, LLC. | Lenoir, NC, United States | Makes it | Serious problems, FDA actionNov 15, 2024 · 12 inspections, 1 with FDA action |
Recalls
- May 5, 2020 · Class III · Exela Pharma Sciences LLC
Short Fill
Lots: Lot #P0000471, Catalog #2020TS002, Exp Date: 04/2021
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Potassium Cation: every company that makes it
- Form
- injection, solution, concentrate
- Strength
- 3.93 g per 20 mL
- Approval
- ANDA ANDA206203
- On the market since
- Jan 7, 2016
- Package NDCs
51754-2001-4- Official label
- DailyMed (National Library of Medicine), updated Jan 7, 2016
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