# Desonide

NDC: 0472-0803
Generic name: desonide
Labeler / Manufacturer: Actavis Pharma, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: LOTION
Routes: TOPICAL
Marketing started: 20090528
Marketing ended: 20280331
FDA application: ANDA072354

## Active ingredients

- DESONIDE: .5 mg/mL

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0472-0803"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0472-0803
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ff5d4cd8-ab4d-4a9e-b84b-445c81eeea99