# PrednisoLONE Sodium Phosphate

NDC: 0121-1100
Generic name: PrednisoLONE Sodium Phosphate
Labeler / Manufacturer: PAI Holdings, LLC dba PAI Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260626

FDA application: NDA019157

## Active ingredients

- PREDNISOLONE SODIUM PHOSPHATE: 5 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0121-1100"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0121-1100
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d1f937e7-fed5-4079-bd52-5d930b34ae9f