# terbinafine hydrochloride

NDC: 71335-9677
Generic name: terbinafine hydrochloride
Labeler / Manufacturer: Bryant Ranch Prepack
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20220128

FDA application: ANDA078163

## Active ingredients

- TERBINAFINE HYDROCHLORIDE: 250 mg/1

## Pharmacological class

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## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"71335-9677"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=71335-9677
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=5a921005-304e-4f5b-b9ba-681749e2499b