# SOLU-MEDROL

NDC: 70518-2023
Generic name: methylprednisolone sodium succinate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20190415

FDA application: NDA011856

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 125 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-2023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-2023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=1d5ef347-2e9a-432f-9a88-a7c4ba300267