# Terbinafine Hydrochloride

NDC: 50090-1048
Generic name: Terbinafine Hydrochloride
Labeler / Manufacturer: A-S Medication Solutions
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

—

## External sources

- openFDA: https://api.fda.gov/drug/ndc.json?search=product_ndc:"50090-1048"
- FDA NDC Directory: https://www.accessdata.fda.gov/scripts/cder/ndc/dsp_searchresult.cfm?p_ndc=50090-1048
- DailyMed: https://dailymed.nlm.nih.gov/dailymed/lookup.cfm?setid=6605103b-fd71-4438-8496-f48973b98901