# Prednisone

NDC: 72189-489
Generic name: Prednisone
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230607

FDA application: ANDA208412

## Active ingredients

- PREDNISONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-489"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-489
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=fd8eb82e-52df-c368-e053-6294a90ac6b0