NDC 70518-2725
Naloxone Hydrochloride 1 mg per 1 mL injection
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. 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 |
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
- May 5, 2020
- Package NDCs
70518-2725-070518-2725-1- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2026
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