NDC 24208-715
Prednisolone Sodium Phosphate 10 mg per 1 mL solution/ drops
On the label: Bausch & Lomb Incorporated.
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Bausch & Lomb Incorporated | Tampa, FL, United States | Makes it | Serious problems, FDA actionMar 20, 2026 · 17 inspections, 3 with FDA action |
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution/ drops, ophthalmic
- Strength
- 10 mg per 1 mL
- Approval
- ANDA ANDA040070
- On the market since
- Jul 29, 1994
- Package NDCs
24208-715-0224208-715-0624208-715-10- Official label
- DailyMed (National Library of Medicine), updated Apr 17, 2023
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