VFEND

NDC 0049-3190 · Roerig

FDA carries 2 listing records for this NDC; the most recent is shown.

Generic namevoriconazole

Dosage formINJECTION, POWDER, LYOPHILIZED, FOR SOLUTION

RouteINTRAVENOUS

Active ingredient(s)VORICONAZOLE

Strength10 mg/mL

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

Marketing categoryNDA

Packages

0049-3190-01 — 1 VIAL, SINGLE-USE in 1 CARTON (0049-3190-01) / 20 mL in 1 VIAL, SINGLE-USE

0049-3190-28 — 1 VIAL, SINGLE-DOSE in 1 CARTON (0049-3190-28) / 20 mL in 1 VIAL, SINGLE-DOSE

Billed under HCPCS

J3465 — Injection, voriconazole, 10 mg Medicare Part B payment limit (ASP + 6%): $0.56

Related Codes

Same active ingredient

FDA lists these products with the same active ingredient.

0049-3160 — voriconazole, 0049-3180 — voriconazole, 0049-4190 — VORICONAZOLE, 0121-1091 — Voriconazole Injection, 0378-1626 — voriconazole, 0378-1640 — voriconazole, 0781-3416 — Voriconazole, 0781-5667 — voriconazole, 0781-5668 — voriconazole, 0904-6596 — voriconazole, 0904-7024 — Voriconazole, 14335-730 — VORICONAZOLE, 16714-198 — Voriconazole, 16714-199 — Voriconazole, 27241-062 — Voriconazole, 27241-063 — Voriconazole, 31722-224 — Voriconazole, 31722-266 — Voriconazole, 40032-038 — voriconazole, 43386-038 — 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.