NDC 72603-590
naloxone hydrochloride 0.4 mg per 1 mL injection, solution
On the label: Northstar Rx LLC..
Where it's 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
- Jul 1, 2024
- Package NDCs
72603-590-0172603-590-1072603-590-25- Official label
- DailyMed (National Library of Medicine), updated Jan 27, 2025
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