NDC 71626-902
Prednisolone Sodium Phosphate 20 mg per 5 mL solution
On the label: Medstone Pharma LLC. It's repackaged: Medstone Pharma LLC rebottles it from Pharmaceutical Associates, Inc.'s NDC 0121-0777.
Where the pills inside were 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
- Strength
- 20 mg per 5 mL
- Approval
- ANDA ANDA078988
- On the market since
- Jan 31, 2017
- Package NDCs
71626-902-05- Official label
- DailyMed (National Library of Medicine), updated Mar 8, 2021
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