# Prednisolone

NDC: 70404-077
Generic name: Prednisolone oral
Labeler / Manufacturer: Tulex Pharmaceuticals Inc
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20260708

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:"70404-077"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70404-077
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=757b41c4-a0fe-4a09-8816-a4cdb7558f41