# PrednisoLONE

NDC: 0527-5406
Generic name: Prednisolone
Labeler / Manufacturer: Lannett Company, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SYRUP
Routes: ORAL
Marketing started: 20070921

FDA application: ANDA040775

## Active ingredients

- PREDNISOLONE: 15 mg/5mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0527-5406"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0527-5406
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=86652e2d-664a-4388-a611-c2a9aa4a4bc8