# Hydrocortisone Butyrate

NDC: 51672-4074
Generic name: Hydrocortisone Butyrate
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20050804

FDA application: ANDA076654

## Active ingredients

- HYDROCORTISONE BUTYRATE: 1 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4074"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4074
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51176835-598d-4da7-8a00-6bd36f52aa82