NDC 70385-2033
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 Somerset Therapeutics, LLC's NDC 70069-071.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Somerset Therapeutics Private Limited | Bengaluru, India | Makes it, tests it, packages it and labels it | Serious problems, FDA actionFeb 21, 2025 · 10 inspections, 4 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, intramuscular; intravenous; subcutaneous
- Strength
- 0.4 mg per 1 mL
- Approval
- ANDA ANDA207633
- On the market since
- Aug 8, 2017
- Package NDCs
70385-2033-1- Official label
- DailyMed (National Library of Medicine), updated Jan 12, 2026
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