NDC 63323-221
Vancomycin Hydrochloride 500 mg per 10 mL injection, powder, lyophilized, for solution
On the label: Fresenius Kabi, LLC.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Fresenius Kabi USA, LLC | Grand Island, NY, United States | Makes it and tests it | Problems found, fixed voluntarilyOct 13, 2023 · 14 inspections, 2 with FDA action |
| Fresenius Kabi USA, LLC | Melrose Park, IL, United States | Makes it and tests it | Problems found, fixed voluntarilyAug 24, 2023 · 13 inspections, 2 with FDA action |
| 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, intravenous
- Strength
- 500 mg per 10 mL
- Approval
- ANDA ANDA062663
- On the market since
- Sep 1, 2000
- Package NDCs
63323-221-0163323-221-10- Official label
- DailyMed (National Library of Medicine), updated May 15, 2025
Got it by mail or from a pharmacy you don't know? Look the pharmacy up on Who Filled My Rx?