# Fluocinonide

NDC: 51672-1386
Generic name: Fluocinonide
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20161027

FDA application: ANDA071500

## Active ingredients

- FLUOCINONIDE: .5 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1386"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1386
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5782d791-48fd-4cee-853d-235eb4d04a40