# Methylprednisolone Sodium Succinate

NDC: 63323-265
Generic name: METHYLPREDNISOLONE SODIUM SUCCINATE
Labeler / Manufacturer: Fresenius Kabi USA, LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20041130

FDA application: ANDA040612

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 1 g/16mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"63323-265"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63323-265
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=c5d22210-73c6-4697-a267-75e243508642