# Prednisolone Sodium Phosphate

NDC: 42799-815
Generic name: Prednisolone Sodium Phosphate
Labeler / Manufacturer: Edenbridge Pharmaceuticals LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20231009

FDA application: ANDA203559

## Active ingredients

- PREDNISOLONE SODIUM PHOSPHATE: 15 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"42799-815"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=42799-815
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1793e218-7b49-497d-879f-1020de6e6d68