NDC 70594-045
Vancomycin Hydrochloride 500 mg injection, powder, 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 |
| Xellia Pharmaceuticals Ltd. | Budapest, Hungary | Tests it | Problems found, fixed voluntarilyJul 30, 2025 · 4 inspections |
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- injection, powder, for solution
- Strength
- 500 mg
- Approval
- ANDA ANDA204107
- On the market since
- Jan 28, 2019
- Package NDCs
70594-045-0170594-045-0270594-045-03- Official label
- DailyMed (National Library of Medicine), updated Feb 25, 2022
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