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Terbinafine Hydrochloride

NDC 68071-1640 · NuCare 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

68071-1640-3 — 30 TABLET in 1 BOTTLE (68071-1640-3)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

56062-080 — Terbinafine Hydrochloride, 59779-080 — Terbinafine Hydrochloride, 59779-523 — Terbinafine Hydrochloride, 60429-222 — Terbinafine Hydrochloride, 60687-909 — Terbinafine Hydrochloride, 61047-120 — Terbinafine Hydrochloride, 61047-139 — Terbinafine hydrochloride, 62135-572 — Terbinafine, 63187-111 — Terbinafine Hydrochloride, 65862-079 — Terbinafine Hydrochloride, 68071-2381 — Terbinafine Tablets 250 mg, 68071-4500 — Terbinafine Hydrochloride, 68071-4873 — Terbinafine Hydrochloride, 68788-4044 — Terbinafine Hydrochloride, 68788-7450 — Terbinafine Hydrochloride, 68788-9814 — Terbinafine Hydrochloride, 69097-731 — Terbinafine Tablets 250 mg, 69097-859 — Terbinafine, 69292-225 — Terbinafine Tablets 250 mg, 69452-351 — 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.