NDC 36000-308
naloxone hydrochloride 0.4 mg per 1 mL injection, solution
On the label: Baxter Healthcare Corporation.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| UBI Pharma Inc. | Hukou, Taiwan | Makes it | Problems found, fixed voluntarilyJun 6, 2023 · 4 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 ANDA214785
- On the market since
- Jan 29, 2021
- Package NDCs
36000-308-0136000-308-10- Official label
- DailyMed (National Library of Medicine), updated Jul 2, 2021
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