NDC 0409-3299
Sodium Acetate 164 mg per 1 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 |
Product details
- Generic drug
- Acetate Ion: every company that makes it
- Form
- injection, solution, concentrate, intravenous
- Strength
- 164 mg per 1 mL
- Approval
- NDA NDA018893
- On the market since
- Apr 30, 2005
- Package NDCs
0409-3299-050409-3299-060409-3299-150409-3299-16- Official label
- DailyMed (National Library of Medicine), updated Mar 26, 2026
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