# TERBINAFINE

NDC: 87564-010
Generic name: terbinafine hydrochloride tablet
Labeler / Manufacturer: Amerisyn LLC
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20260803

FDA application: ANDA076390

## 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:"87564-010"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=87564-010
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=584d1fae-0120-49a0-e063-6394a90a36fc