# Prednisone

NDC: 55154-2147
Generic name: Prednisone
Labeler / Manufacturer: Cardinal Health 107, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250709
Marketing ended: 20270331
FDA application: ANDA040392

## 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:"55154-2147"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55154-2147
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=199ed6a6-d9d9-49de-b383-5933a026591b