# PredniSONE Tablets, USP, 20 mg

NDC: 72162-2486
Generic name: PredniSONE
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20240306

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:"72162-2486"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72162-2486
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=48ee895b-dc3a-4f1f-8688-e06c217f449b