NDC 45932-0028
Vancomycin Hydrochloride 500 mg injection, powder, lyophilized, for solution
On the label: Xellia Pharmaceuticals, ApS.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Xellia Pharmaceuticals ApS | Copenhagen S, Denmark | Makes 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
- 500 mg
- Approval
- ANDA ANDA091377
- On the market since
- Apr 10, 2014
- Package NDCs
45932-0028-145932-0028-2- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2015
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