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Voriconazole

NDC 65862-891 · Aurobindo Pharma Limited

Generic nameVoriconazole
Dosage formTABLET, FILM COATED
RouteORAL
Active ingredient(s)VORICONAZOLE
Strength50 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

65862-891-01 — 100 TABLET, FILM COATED in 1 BOTTLE (65862-891-01)

65862-891-03 — 3 BLISTER PACK in 1 CARTON (65862-891-03) / 10 TABLET, FILM COATED in 1 BLISTER PACK (65862-891-10)

65862-891-05 — 500 TABLET, FILM COATED in 1 BOTTLE (65862-891-05)

65862-891-30 — 30 TABLET, FILM COATED in 1 BOTTLE (65862-891-30)

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

55150-321 — Voriconazole, 59762-0935 — Voriconazole, 60687-273 — Voriconazole, 60687-968 — Voriconazole, 60687-979 — Voriconazole, 63629-8734 — voriconazole, 65162-913 — Voriconazole, 65219-190 — Voriconazole, 65841-830 — voriconazole, 65841-831 — voriconazole, 65862-892 — Voriconazole, 68083-321 — Voriconazole, 68462-572 — voriconazole, 68462-573 — voriconazole, 70436-029 — voriconazole, 70436-230 — voriconazole, 70594-067 — Voriconazole, 71288-027 — Voriconazole, 71335-2911 — voriconazole, 72162-1198 — 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.