# Terbinafine Hydrochloride

NDC: 60429-222
Generic name: Terbinafine Hydrochloride
Labeler / Manufacturer: Golden State Medical Supply, Inc.
Product type: HUMAN PRESCRIPTION DRUG
Marketing category: Abbreviated NDA (generic)
Dosage form: TABLET
Routes: ORAL
Marketing started: 20100604
Marketing ended: 20270531
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:"60429-222"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=60429-222
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=b43e4644-024c-4aa6-b403-19152c785802