# Desonide

NDC: 51672-4079
Generic name: Desonide
Labeler / Manufacturer: Taro Pharmaceuticals U.S.A., Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20141031

FDA application: ANDA202161

## Active ingredients

- DESONIDE: .5 mg/mL

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-4079"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-4079
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=af607c32-3da9-4fbe-99e7-4934a5c8d8f0