# Methylprednisolone Sodium Succinate

NDC: 55150-262
Generic name: Methylprednisolone Sodium Succinate
Labeler / Manufacturer: Eugia US LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20151215

FDA application: ANDA207667

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 40 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"55150-262"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=55150-262
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2035f00e-2299-473a-b004-cb93f541cfa9