United States · FDA National Drug Code directory

Terbinafine Hydrochloride

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
68788-9814_02fc7642-968f-4ddf-a86a-146ed1a40162
Product NDC
68788-9814
Form
CREAM
Composition / generic term
Terbinafine Hydrochloride
Labeler
Preferred Pharmaceuticals, Inc
Marketing category
ANDA
Marketing start / end (source format)
20120405
Source listing expiry
20261231

Source-listed ingredients

  • TERBINAFINE HYDROCHLORIDE — 1 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 15 g in 1 TUBE (68788-9814-1) · 68788-9814-1

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 →