United States · FDA National Drug Code directory

Voriconazole

A source-listed medicine record.

Factual source checks only. This page is not a clinically reviewed monograph. Historical or discontinued records may be included; listing does not confirm approval, current availability or pharmacy stock.

Medicine identity

Source reference
70594-067_794911b6-dd66-445a-b73d-5037552e0b94
Product NDC
70594-067
Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Composition / generic term
Voriconazole
Labeler
Xellia Pharmaceuticals USA LLC
Marketing category
NDA
Marketing start / end (source format)
20230824
Source listing expiry
20261231

Source-listed ingredients

  • VORICONAZOLE — 10 mg/mL

These values do not establish equivalence or a dose recommendation.

Packages

  • 1 VIAL, SINGLE-DOSE in 1 CARTON (70594-067-01) / 20 mL in 1 VIAL, SINGLE-DOSE · 70594-067-01

Source and coverage

Open FDA National Drug Code directory

Snapshot retrieved: 2026-09-17. This is the acquisition date, not a medical review date.

Clinical information, images and comparisons appear only when separately reviewed for this record. Coverage may be incomplete. Ask a pharmacist or clinician about your treatment.

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Voriconazole — United States | Molindra Medicines