NDC 69238-2122
Prednisolone Sodium Phosphate 15 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 |
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution, oral
- Strength
- 15 mg per 5 mL
- Approval
- ANDA ANDA216715
- On the market since
- Oct 27, 2022
- Package NDCs
69238-2122-9- Official label
- DailyMed (National Library of Medicine), updated Apr 29, 2025
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