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Voriconazole

NDC 60687-979 · American Health Packaging

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

60687-979-21 — 30 BLISTER PACK in 1 CARTON (60687-979-21) / 1 TABLET, FILM COATED in 1 BLISTER PACK (60687-979-11)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

43547-378 — Voriconazole, 48433-146 — voriconazole, 48433-147 — voriconazole, 50268-803 — Voriconazole, 51079-164 — voriconazole, 51079-165 — voriconazole, 55150-321 — Voriconazole, 59762-0935 — Voriconazole, 60687-273 — Voriconazole, 60687-968 — 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, 68462-573 — voriconazole, +36 more

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