NDC 68462-477
Vancomycin Hydrochloride 750 mg injection, powder, lyophilized, for solution
On the label: Glenmark Pharmaceuticals Inc., USA.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Gland Pharma Limited | Hyderabad, India | Makes it, tests it, packages it and labels it | Problems found, fixed voluntarilyJun 27, 2023 · 4 inspections |
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- injection, powder, lyophilized, for solution, intravenous
- Strength
- 750 mg
- Approval
- ANDA ANDA218140
- On the market since
- Mar 21, 2025
- Package NDCs
68462-477-2068462-477-74- Official label
- DailyMed (National Library of Medicine), updated Dec 23, 2025
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