# Hydrocortisone sodium succinate

NDC: 70771-1966
Generic name: Hydrocortisone sodium succinate
Labeler / Manufacturer: Zydus Lifesciences Limited
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: INJECTION
Routes: INTRAMUSCULAR, INTRAVENOUS
Marketing started: 20260509

FDA application: ANDA217191

## 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:"70771-1966"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=70771-1966
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=d533ebee-9f1c-42d7-9808-ae5d5e55741b