NDC 51662-1671
Naloxone Hydrochloride 0.4 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 Hikma Pharmaceuticals USA Inc.'s NDC 0641-6132.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hikma Pharmaceuticals USA Inc. | Cherry Hill, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundMay 13, 2026 · 18 inspections |
Repackaging site
- HF Acquisition Co LLC, Mukilteo, WA, United States · relabels it
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA070299
- On the market since
- Sep 24, 1986
- Package NDCs
51662-1671-151662-1671-3- Official label
- DailyMed (National Library of Medicine), updated Aug 5, 2025
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