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Terbinafine

NDC 71205-492 · Proficient Rx LP

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

Packages

71205-492-30 — 30 TABLET in 1 BOTTLE (71205-492-30)

71205-492-35 — 35 TABLET in 1 BOTTLE (71205-492-35)

71205-492-42 — 42 TABLET in 1 BOTTLE (71205-492-42)

71205-492-45 — 45 TABLET in 1 BOTTLE (71205-492-45)

71205-492-60 — 60 TABLET in 1 BOTTLE (71205-492-60)

71205-492-90 — 90 TABLET in 1 BOTTLE (71205-492-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

69452-351 — terbinafine hydrochloride, 70000-0338 — Terbinafine Hydrochloride, 70518-2941 — Terbinafine Hydrochloride, 70518-3907 — terbinafine hydrochloride, 70518-4323 — Terbinafine, 70518-4421 — Terbinafine, 70677-1003 — Terbinafine Hydrochloride, 71205-061 — Terbinafine Hydrochloride, 71205-127 — Terbinafine Hydrochloride, 71205-152 — Terbinafine, 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, 72789-394 — Terbinafine Hydrochloride, 73469-7215 — Terbinafine Hydrochloride, 76282-209 — Terbinafine, +55 more

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