# prednisone

NDC: 80425-0484
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: 20250131

FDA application: ANDA208412

## Active ingredients

- PREDNISONE: 10 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"80425-0484"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=80425-0484
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d0562ad-6175-833c-e063-6394a90ad029