# Terbinafine Hydrochloride

NDC: 51672-2140
Generic name: Terbinafine Hydrochloride
Labeler / Manufacturer: Sun Pharmaceutical Industries, Inc.
Product type: HUMAN OTC DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: CREAM
Routes: TOPICAL
Marketing started: 20070702

FDA application: ANDA077511

## Active ingredients

- TERBINAFINE HYDROCHLORIDE: 1 g/100g

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"51672-2140"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=51672-2140
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=ca9cd2bd-4805-4469-b754-01a7487b71a6