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
0363-4502_3996583d-a3da-fa4a-e063-6394a90af78a
Product NDC
0363-4502
Form
CREAM
Composition / generic term
Terbinafine Hydrochloride
Labeler
WALGREEN COMPANY
Marketing category
ANDA
Marketing start / end (source format)
20231025
Source listing expiry
20261231

Source-listed ingredients

  • TERBINAFINE HYDROCHLORIDE — 1 g/100g

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 TUBE in 1 CARTON (0363-4502-02) / 30 g in 1 TUBE · 0363-4502-02

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.

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