NDC 51662-1597
Gentamicin Sulfate 40 mg per 1 mL injection, solution
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from Hospira, Inc.'s NDC 0409-1207.
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 |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- May 2, 2013 · Class II · Hospira Inc.
Presence of Particulate Matter: visible particles were identified floating in the primary container.
Lots: Lot 07-067-DK Exp. 07/13
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Gentamicin: every company that makes it
- Form
- injection, solution, intramuscular; intravenous
- Strength
- 40 mg per 1 mL
- Approval
- ANDA ANDA062420
- On the market since
- Oct 1, 2022
- Package NDCs
51662-1597-251662-1597-3- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2024
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