NDC 71335-2938
PredniSONE Tablets, USP, 20 mg 20 mg tablet
On the label: Bryant Ranch Prepack. It's repackaged: Bryant Ranch Prepack 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
- Bryant Ranch Prepack, Burbank, CA, United States · repackages it and relabels 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
71335-2938-171335-2938-2- Official label
- DailyMed (National Library of Medicine), updated Mar 11, 2026
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