NDC 72789-509
PredniSONE Tablets, USP, 20 mg 20 mg tablet
On the label: PD-Rx Pharmaceuticals, Inc.. It's repackaged: PD-Rx Pharmaceuticals, Inc. rebottles it from Granulation Technology, Inc.'s NDC 63561-0122.
Where the pills inside were made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granulation Technology, Inc. | Fairfield, NJ, United States | Makes it | Not inspected on record |
Repackaging site
- PD-Rx Pharmaceuticals Inc., Oklahoma City, OK, United States · repackages it
Product details
- Generic drug
- Prednisone: every company that makes it
- Form
- tablet, oral
- Strength
- 20 mg
- Approval
- ANDA ANDA212629
- On the market since
- May 22, 2025
- Package NDCs
72789-509-0672789-509-0972789-509-1272789-509-15- Official label
- DailyMed (National Library of Medicine), updated Jun 4, 2026
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