NDC 70518-4785
naloxone hydrochloride 0.4 mg per 1 mL injection, solution
On the label: Remedyrepack Inc.. It's repackaged: Remedyrepack Inc. rebottles it from Lifestar Pharma LLC.'s NDC 70756-658.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Mankind Pharma Limited | Sirmaur, India | Makes it, tests it and packages it | Problems found, fixed voluntarilyFeb 25, 2022 · 2 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 ANDA218404
- On the market since
- Oct 28, 2026
- Package NDCs
70518-4785-070518-4785-1- Official label
- DailyMed (National Library of Medicine), updated Nov 2, 2026
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