# Prednisolone Sodium Phosphate

NDC: 62135-330
Generic name: prednisolone sodium phosphate
Labeler / Manufacturer: Chartwell RX, LLC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20040525

FDA application: ANDA075988

## 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:"62135-330"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-330
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2d8c861d-3756-4b75-aaa9-1b82cf11eb94