# Prednisone

NDC: 71335-3129
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: 20041221

FDA application: ANDA040584

## Active ingredients

- PREDNISONE: 1 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-3129"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-3129
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e4c1c8c5-0aa1-4531-aa7a-8567ac8dcba8