# PredniSONE

NDC: 63187-243
Generic name: PredniSONE
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20030314

FDA application: ANDA084283

## Active ingredients

- PREDNISONE: 50 mg/1

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-243"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-243
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e109f428-ca85-4a2c-acd0-ca8d498e7723