NDC 0409-7299
Sodium Acetate 3.28 g per 20 mL injection, solution, concentrate
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
| Pfizer Healthcare India Private Limited | Anakapalli, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyOct 18, 2022 · 7 inspections, 1 with FDA action |
Recalls
- Feb 26, 2013 · Class II · Hospira Inc.
Lack of Assurance of Sterility: Loose crimp applied to the fliptop vial.
Lots: Lot 23-320-DK and 23-321-DK Exp. 11/14
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Sodium Cation: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 3.28 g per 20 mL
- Approval
- NDA NDA018893
- On the market since
- Mar 31, 2005
- Package NDCs
0409-7299-730409-7299-83- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2026
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