# Prednisolone

NDC: 62135-250
Generic name: Prednisolone oral
Labeler / Manufacturer: Chartwell RX, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20221120

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:"62135-250"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62135-250
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=aa40f582-cced-4e6e-90f0-10ab310ab2a7