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
- 0121-1091_16f323c7-0e2e-4066-8dbf-bbeb11788533
- Product NDC
- 0121-1091
- Form
- INJECTION
- Composition / generic term
- Voriconazole Injection
- Labeler
- PAI Holdings, LLC dba PAI Pharma
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20260514
- Source listing expiry
- 20271231
Source-listed ingredients
- VORICONAZOLE — 10 mg/mL
These values do not establish equivalence or a dose recommendation.
Packages
- 1 VIAL, SINGLE-USE in 1 CARTON (0121-1091-55) / 20 mL in 1 VIAL, SINGLE-USE · 0121-1091-55
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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