# Desonide

NDC: 0713-0661
Generic name: Desonide
Labeler / Manufacturer: Cosette Pharmaceuticals, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20160819

FDA application: ANDA074027

## Active ingredients

- DESONIDE: .5 mg/g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"0713-0661"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=0713-0661
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=51e39fd1-2ae7-9ed6-5f24-c4656dd97f0b