# Methylprednisolone Sodium Succinate

NDC: 70121-1001
Generic name: Methylprednisolone
Labeler / Manufacturer: Amneal Pharmaceuticals LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20161111

FDA application: ANDA207549

## 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:"70121-1001"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70121-1001
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=e86fbda8-00e4-4d54-841a-59dea6c15e70