# Methylprednisolone Sodium Succinate

NDC: 70518-4345
Generic name: Methylprednisolone Sodium Succinate
Labeler / Manufacturer: REMEDYREPACK INC.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20250527

FDA application: ANDA203125

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 125 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"70518-4345"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70518-4345
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ae524bdb-9fd0-49f9-802d-465a374c175b