# Methylprednisolone Sodium Succinate

NDC: 0143-9850
Generic name: Methylprednisolone Sodium Succinate
Labeler / Manufacturer: Hikma Pharmaceuticals USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20160101

FDA application: ANDA202691

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 500 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0143-9850"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0143-9850
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=2e540674-0915-4498-8e2b-751c7e97532a