United States · FDA National Drug Code directory
Terbinafine
A source-listed medicine record.
Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.
Medicine identity
- Source reference
- 76282-209_dc86cdd6-0a8a-4e5c-b3c4-8b05388af862
- Product NDC
- 76282-209
- Form
- TABLET
- Composition / generic term
- Terbinafine
- Labeler
- Exelan Pharmaceuticals Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20120425
- Source listing expiry
- 20261231
Source-listed ingredients
- TERBINAFINE HYDROCHLORIDE — 250 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET in 1 BOTTLE (76282-209-01) · 76282-209-01
- 500 TABLET in 1 BOTTLE (76282-209-05) · 76282-209-05
- 30 TABLET in 1 BOTTLE (76282-209-30) · 76282-209-30
Source and coverage
Open FDA National Drug Code directory →
Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.
Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.
Browse United States records →