# Hydrocortisone Butyrate

NDC: 68682-271
Generic name: hydrocortisone butyrate
Labeler / Manufacturer: Oceanside Pharmaceuticals
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20090901

FDA application: NDA018652

## Active ingredients

- HYDROCORTISONE BUTYRATE: 1 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"68682-271"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=68682-271
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=7c3f8417-7861-41e3-876f-9b82aff7d1a0