# Terbinafine Hydrochloride

NDC: 63629-1993
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: 20101227

FDA application: ANDA077714

## 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:"63629-1993"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=63629-1993
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=facaea7f-cb4d-410f-85e4-e1ac9ff565ac