# PredniSONE Tablets, USP, 20 mg

NDC: 72789-500
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: 20 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-500"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-500
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3befbdc5-7d20-41b6-ad80-98e1c6b8caf5