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Terbinafine

NDC 72789-394 · PD-Rx Pharmaceuticals, Inc.

Generic nameTerbinafine Hydrochloride
Dosage formTABLET
RouteORAL
Active ingredient(s)TERBINAFINE HYDROCHLORIDE
Strength250 mg/1
Pharmacologic classAllylamine Antifungal [EPC], Allylamine [CS]
Marketing categoryANDA

Packages

72789-394-42 — 42 TABLET in 1 BOTTLE, PLASTIC (72789-394-42)

72789-394-90 — 90 TABLET in 1 BOTTLE, PLASTIC (72789-394-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

71205-127 — Terbinafine Hydrochloride, 71205-152 — Terbinafine, 71205-492 — Terbinafine Hydrochloride, 71335-0918 — Terbinafine Hydrochloride, 71335-1124 — Terbinafine Hydrochloride, 71335-9677 — terbinafine hydrochloride, 72162-1595 — Terbinafine Hydrochloride, 72162-2539 — Terbinafine Hydrochloride, 72189-243 — TERBINAFINE, 72559-035 — Terbinafine Hydrochloride, 73469-7215 — Terbinafine Hydrochloride, 76282-209 — Terbinafine, 82804-220 — terbinafine hydrochloride, 83818-024 — TINEA VERSICOLOR Cream, 84485-3605 — terbinafine hydrochloride, 84485-3606 — terbinafine hydrochloride, 84485-3607 — Terbinafine Hydrochloride, 84485-3748 — Terbinafine Hydrochloride, 84485-4030 — Terbinafine Hydrochloride, 85398-006 — Terbinafine Hydrochloride, +55 more

From the FDA National Drug Code Directory, retrieved August 24, 2026. Product listings are submitted by labelers; FDA does not verify them.