# SOLU-MEDROL

NDC: 51662-1264
Generic name: SOLU-MEDROL
Labeler / Manufacturer: HF Acquisition Co. LLC, DBA HealthFirst
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20180902

FDA application: NDA011856

## Active ingredients

- METHYLPREDNISOLONE SODIUM SUCCINATE: 40 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1264"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1264
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74e5060c-8426-1b77-e053-2a91aa0a1f13