NDC 51662-1239
Naloxone Hydrochloride 1 mg per 1 mL injection
On the label: HF Acquisition Co. LLC. DBA HealthFirst. It's repackaged: HF Acquisition Co. LLC. DBA HealthFirst rebottles it from International Medication Systems, Ltd.'s NDC 76329-3369.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| International Medication Systems, Ltd. | South El Monte, CA, United States | Makes it and tests it | Serious problems, FDA actionDec 19, 2025 · 15 inspections, 1 with FDA action |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, parenteral
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA072076
- On the market since
- Sep 3, 2018
- Package NDCs
51662-1239-151662-1239-251662-1239-3- Official label
- DailyMed (National Library of Medicine), updated Jan 25, 2024
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