NDC 69238-2261
Vancomycin Hydrochloride 250 mg per 5 mL solution
On the label: Amneal Pharmaceuticals.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Amneal Pharmaceuticals, LLC | Branchburg, NJ, United States | Makes it, tests it, packages it and labels it | No problems foundAug 28, 2026 · 9 inspections |
Recalls
- Mar 21, 2024 · Class I · Amneal Pharmaceuticals of New York, LLC
Superpotent Drug: Due to overfilling of drug powder
Lots: Lot # (a) 22613003A, Exp. date 09/30/2025; (b) 22613004A, 22613005A, Exp. date 09/30/2025; (c) 22613005B, Exp. date 09/30/2025
Class I recalls are the most serious; Class III the least. A recall covers specific lots, listed on each recall.
Product details
- Generic drug
- Vancomycin: every company that makes it
- Form
- solution, oral
- Strength
- 250 mg per 5 mL
- Approval
- ANDA ANDA215338
- On the market since
- Jun 26, 2023
- Package NDCs
69238-2261-369238-2261-569238-2261-7- Official label
- DailyMed (National Library of Medicine), updated Jun 23, 2023
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