# Prednisolone Sodium Phosphate

NDC: 13925-166
Generic name: Prednisolone Sodium Phosphate
Labeler / Manufacturer: Seton Pharmaceuticals, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20131018

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:"13925-166"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=13925-166
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=833ba492-8823-43b4-9a91-8b28d94a740b