# PredniSONE Tablets, USP, 5 mg

NDC: 72789-498
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: 5 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72789-498"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72789-498
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=251e9fe7-b1f5-4b5b-b5fa-8c8be43e284e