NDC 63561-0120
PredniSONE Tablets, USP, 5 mg 5 mg tablet
On the label: Granulation Technology, Inc..
Where it's made
| Factory | Where | Role | Last FDA inspection |
|---|---|---|---|
| Granulation Technology, Inc. | Fairfield, NJ, United States | Makes it | Not inspected on record |
Product details
- Generic drug
- Prednisone: every company that makes it
- Form
- tablet, oral
- Strength
- 5 mg
- Approval
- ANDA ANDA212629
- On the market since
- May 22, 2025
- Package NDCs
63561-0120-163561-0120-263561-0120-5- Official label
- DailyMed (National Library of Medicine), updated Aug 15, 2025
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