# Prednisolone Sodium Phosphate

NDC: 63187-215
Generic name: Prednisolone Sodium Phosphate
Labeler / Manufacturer: Proficient Rx LP
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20050425

FDA application: ANDA076913

## Active ingredients

- PREDNISOLONE SODIUM PHOSPHATE: 15 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63187-215"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63187-215
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=14b7f41b-4df1-42cb-bd1b-c74b28de2670