NDC 51662-1508
Gentamicin 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 Fresenius Kabi, LLC's NDC 63323-010.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Nov 12, 2014 · Class II · Fresenius Kabi USA, LLC
Defective Container: Vials may be missing stoppers.
Lots: Product Code: 1020; NDC: 63323-010-20; Lot Number: 6107992; Expiration Date: 09/2015
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 ANDA062366
- On the market since
- May 10, 2021
- Package NDCs
51662-1508-251662-1508-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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