voriconazole

NDC 68462-573 · Glenmark Pharmaceuticals Inc., USA

Generic namevoriconazole

Dosage formTABLET, FILM COATED

RouteORAL

Active ingredient(s)VORICONAZOLE

Strength200 mg/1

Pharmacologic classAzole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]

Marketing categoryANDA

Packages

68462-573-13 — 3 BLISTER PACK in 1 CARTON (68462-573-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK

68462-573-30 — 30 TABLET, FILM COATED in 1 BOTTLE (68462-573-30)

68462-573-90 — 90 TABLET, FILM COATED in 1 BOTTLE (68462-573-90)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

60687-979 — Voriconazole, 63629-8734 — voriconazole, 65162-913 — Voriconazole, 65219-190 — Voriconazole, 65841-830 — voriconazole, 65841-831 — voriconazole, 65862-891 — Voriconazole, 65862-892 — Voriconazole, 68083-321 — Voriconazole, 68462-572 — voriconazole, 70436-029 — voriconazole, 70436-230 — voriconazole, 70594-067 — Voriconazole, 71288-027 — Voriconazole, 71335-2911 — voriconazole, 72162-1198 — voriconazole, 72266-131 — Voriconazole, 72572-875 — Voriconazole, 72578-062 — voriconazole, 72578-063 — voriconazole, +36 more

From the FDA National Drug Code Directory, retrieved 2026-08-24. Product listings are submitted by labelers; FDA does not verify them.