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
- 72843-441_37fd1318-4e96-c496-e063-6394a90a90e3
- Product NDC
- 72843-441
- Form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Composition / generic term
- voriconazole
- Labeler
- UBI Pharma Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20200831
- Source listing expiry
- 20261231
Source-listed ingredients
- VORICONAZOLE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 20 mL in 1 VIAL, SINGLE-USE (72843-441-01) · 72843-441-01
Source and coverage
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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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