# Prednisone

NDC: 71335-2160
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: 20191115

FDA application: ANDA211575

## Active ingredients

- PREDNISONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-2160"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-2160
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c60a07f9-ed9f-4434-a69d-2e2fea4843fd