# Desoximetasone

NDC: 51672-1352
Generic name: Desoximetasone
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 19850117

FDA application: NDA018594

## Active ingredients

- DESOXIMETASONE: .5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1352"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1352
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=96898d55-aa50-4281-8c23-ec4738ede394