NDC 0409-1319
Vancomycin Hydrochloride 500 mg per 5 mL injection, powder, lyophilized, for solution
On the label: Hospira, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Hospira, Inc. | McPherson, KS, United States | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJan 17, 2025 · 16 inspections, 2 with FDA action |
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 500 mg per 5 mL
- Approval
- ANDA ANDA063076
- On the market since
- Nov 2, 2021
- Package NDCs
0409-1319-01- Official label
- DailyMed (National Library of Medicine), updated Jan 16, 2025
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