# Desonide

NDC: 16714-729
Generic name: Desonide
Labeler / Manufacturer: NORTHSTAR RX LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 19920630

FDA application: ANDA073548

## 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:"16714-729"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=16714-729
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=0665dd04-1d0b-45bf-90e4-c6e0bd90956d