NDC 55154-2364
Furosemide 10 mg per 1 mL injection, solution
On the label: Cardinal Health 107, LLC. It's repackaged: Cardinal Health 107, LLC rebottles it from Hospira, Inc.'s NDC 0409-6102.
Where the pills inside were 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 20-564-DK Exp. 02/14 - Jan 10, 2013 · Class II · Hospira, Inc.
Lack of Assurance of Sterility; possible loose crimp applied to fliptop vial
Lots: 18-099-DK
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Furosemide: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 10 mg per 1 mL
- Approval
- NDA NDA018667
- On the market since
- Jul 13, 2010
- Package NDCs
55154-2364-5- Official label
- DailyMed (National Library of Medicine), updated May 6, 2026
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