NDC 51662-1531
Epinephrine 0.1 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 0409-4933.
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 |
| Hospira, Inc. | Location not on file | Tests it | Not inspected on record |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Recalls
- Aug 4, 2025 · Class II · Pfizer Inc
Lack of Assurance of Sterility.
Lots: Lot #: LY3681, LY4360, LY4416, Exp. 02/28/2026
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Epinephrine: every company that makes it
- Form
- injection, solution, intravenous
- Strength
- 0.1 mg per 1 mL
- Approval
- NDA NDA209359
- On the market since
- Apr 25, 2021
- Package NDCs
51662-1531-151662-1531-251662-1531-3- Official label
- DailyMed (National Library of Medicine), updated Jan 30, 2024
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