# Naftifine Hydrochloride

NDC: 51672-1376
Generic name: Naftifine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: GEL
Routes: TOPICAL
Marketing started: 20230401

FDA application: ANDA208201

## Active ingredients

- NAFTIFINE HYDROCHLORIDE: 20 mg/g

## Pharmacological class

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-1376"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-1376
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=92d3ec30-2176-49cd-8a70-668ef65e7663