# Naftin

NDC: 83107-023
Generic name: Naftifine Hydrochloride
Labeler / Manufacturer: Legacy Pharma USA Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: New Drug Application (innovator)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20250729

FDA application: NDA204286

## Active ingredients

- NAFTIFINE HYDROCHLORIDE: 2 g/100g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"83107-023"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=83107-023
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6c6ee055-4031-45a7-8561-ccd989343580