NDC 76045-114
Naloxone Hydrochloride 0.4 mg per 1 mL injection, solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Wilson, NC, United States | Makes it and tests it | Problems found, fixed voluntarilyFeb 13, 2026 · 5 inspections |
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA213573
- On the market since
- Apr 2, 2024
- Package NDCs
76045-114-0176045-114-10- Official label
- DailyMed (National Library of Medicine), updated Jul 31, 2025
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