# PredniSONE

NDC: 17856-3722
Generic name: PredniSONE
Labeler / Manufacturer: Atlantic Biologicals Corps
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 19861213

FDA application: ANDA088703

## Active ingredients

- PREDNISONE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"17856-3722"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=17856-3722
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=07be390e-ef1e-4bf9-a9da-4338b5f6cfa5