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
- 0781-5667_efbbf86a-b798-4963-8786-0d7033ee908b
- Product NDC
- 0781-5667
- Form
- TABLET, FILM COATED
- Composition / generic term
- voriconazole
- Labeler
- Sandoz Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20111212
- Source listing expiry
- 20271231
Source-listed ingredients
- VORICONAZOLE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 500 TABLET, FILM COATED in 1 BOTTLE (0781-5667-05) · 0781-5667-05
- 1000 TABLET, FILM COATED in 1 BOTTLE (0781-5667-10) · 0781-5667-10
- 10 BLISTER PACK in 1 CARTON (0781-5667-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK (0781-5667-06) · 0781-5667-13
- 30 TABLET, FILM COATED in 1 BOTTLE (0781-5667-31) · 0781-5667-31
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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