NDC 70594-048
Vancomycin Hydrochloride 10 g injection, powder, lyophilized, for solution
On the label: Xellia Pharmaceuticals USA LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Xellia Pharmaceuticals ApS | Copenhagen S, Denmark | Makes it, makes the active ingredient, tests it, packages it and labels it | Problems found, fixed voluntarilyDec 4, 2025 · 8 inspections |
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- injection, powder, lyophilized, for solution
- Strength
- 10 g
- Approval
- ANDA ANDA204125
- On the market since
- Oct 1, 2018
- Package NDCs
70594-048-01- Official label
- DailyMed (National Library of Medicine), updated Sep 15, 2023
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