# Prednisolone

NDC: 23155-927
Generic name: prednisolone oral solution
Labeler / Manufacturer: Heritage Pharma Labs Inc. d/b/a Avet Pharmaceuticals Labs Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20250301

FDA application: ANDA040323

## 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:"23155-927"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=23155-927
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b079834f-9aa3-4db9-bd53-de28e8f81c04