# SOLU-CORTEF

NDC: 51662-1261
Generic name: SOLU-CORTEF
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: 20180903

FDA application: NDA009866

## Active ingredients

- HYDROCORTISONE SODIUM SUCCINATE: 100 mg/2mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51662-1261"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51662-1261
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=74f84173-a43f-7788-e053-2991aa0a8fb2