# PredniSONE Tablets, USP, 10 mg

NDC: 72789-513
Generic name: PredniSONE
Labeler / Manufacturer: PD-Rx Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250522

FDA application: ANDA212629

## Active ingredients

- PREDNISONE: 10 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-513"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-513
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bb32e309-e3c7-4009-bcd4-d97545b7e975