# Prednisone

NDC: 72189-430
Generic name: Prednisone
Labeler / Manufacturer: Direct_Rx
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20230303

FDA application: ANDA208412

## Active ingredients

- PREDNISONE: 20 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"72189-430"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=72189-430
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=f6051257-2144-4487-e053-2995a90a973b