NDC 70385-2013
Naloxone Hydrochloride 0.4 mg per 1 mL injection, solution
On the label: Sina Health Inc. It's repackaged: Sina Health Inc rebottles it from Hospira, Inc.'s NDC 0409-1215.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | Rocky Mount, NC, United States | Makes it, tests it, packages it and labels it | No problems foundFeb 7, 2025 · 11 inspections, 3 with FDA action |
Repackaging site
- Sina Health Inc, Scottsdale, AZ, United States · repackages it
Product details
- Generic drug
- Naloxone: every company that makes it
- Form
- injection, solution
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA070256
- On the market since
- Jan 7, 1987
- Package NDCs
70385-2013-1- Official label
- DailyMed (National Library of Medicine), updated Feb 4, 2019
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