# Prednisone

NDC: 80425-0486
Generic name: Prednisone
Labeler / Manufacturer: Advanced Rx of Tennessee, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20250317

FDA application: ANDA211575

## 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:"80425-0486"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0486
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=30956dd5-fe19-d5a9-e063-6394a90a2549