# prednisoLONE sodium phosphate

NDC: 81033-021
Generic name: prednisoLONE sodium phosphate
Labeler / Manufacturer: Kesin Pharma
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: ORAL
Marketing started: 20231027

FDA application: ANDA203559

## Active ingredients

- PREDNISOLONE SODIUM PHOSPHATE: 15 mg/5mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"81033-021"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=81033-021
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=4c0dcbfd-2848-9bd0-e063-6394a90af5a7