NDC 55150-345
Naloxone Hydrochloride 1 mg per 1 mL injection, solution
On the label: AuroMedics Pharma LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Eugia Pharma Specialities Limited | Sangareddy, India | Makes it, tests it and packages it | Serious problems, FDA actionFeb 6, 2026 · 7 inspections, 2 with FDA action |
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, solution, intramuscular; intravenous; subcutaneous
- Strength
- 1 mg per 1 mL
- Approval
- ANDA ANDA213279
- On the market since
- Jan 14, 2021
- Package NDCs
55150-345-0155150-345-10- Official label
- DailyMed (National Library of Medicine), updated May 14, 2025
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