NDC 0121-0773
Prednisolone Sodium Phosphate 10 mg per 5 mL solution
On the label: Pharmaceutical Associates, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| PAI Holdings, LLC dba Pharmaceutical Associates, Inc. and dba PAI Pharma | Greenville, SC, United States | Makes it | No problems foundAug 1, 2025 · 18 inspections, 1 with FDA action |
Product details
- Generic drug
- Prednisolone: every company that makes it
- Form
- solution, oral
- Strength
- 10 mg per 5 mL
- Approval
- ANDA ANDA078465
- On the market since
- Jan 31, 2017
- Package NDCs
0121-0773-08- Official label
- DailyMed (National Library of Medicine), updated Feb 10, 2025
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