# Desonide

NDC: 62332-485
Generic name: Desonide
Labeler / Manufacturer: Alembic Pharmaceuticals Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: OINTMENT
Routes: TOPICAL
Marketing started: 20191024

FDA application: ANDA212473

## 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:"62332-485"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=62332-485
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=9eade7ae-effc-49b5-af7d-8caa183ff252