# Hydrocortisone sodium succinate

NDC: 60505-6411
Generic name: Hydrocortisone sodium succinate
Labeler / Manufacturer: Apotex Corp.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION, POWDER, FOR SOLUTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20260619

FDA application: ANDA219856

## Active ingredients

- HYDROCORTISONE SODIUM SUCCINATE: 100 mg/2mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"60505-6411"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60505-6411
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=bfe185a6-b657-2fbb-4ac2-e085373f15f3