# Prednisolone

NDC: 52817-860
Generic name: Prednisolone oral
Labeler / Manufacturer: TRUPHARMA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260804

FDA application: ANDA219509

## Active ingredients

- PREDNISOLONE: 15 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"52817-860"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=52817-860
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4f83514d-5342-4748-a0d3-b0306ca303c8