# Prednisolone Sodium Phosphate

NDC: 67296-2134
Generic name: Prednisolone Sodium Phosphate
Labeler / Manufacturer: Redpharm Drug
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

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"67296-2134"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=67296-2134
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=3253b63b-0533-6cdc-e063-6294a90aa311