# Hydrocortisone and Acetic Acid

NDC: 51672-3007
Generic name: Hydrocortisone and Acetic Acid
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: SOLUTION
Routes: AURICULAR (OTIC)
Marketing started: 20050428

FDA application: ANDA088759

## Active ingredients

- ACETIC ACID: 20.8 mg/mL
- HYDROCORTISONE: 10.4 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-3007"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-3007
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6383c722-84e2-4719-a13d-19c54e3eefff