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
- 72578-062_66fc1497-5ec6-40b6-b77c-9decfe476c9c
- Product NDC
- 72578-062
- Form
- TABLET, FILM COATED
- Composition / generic term
- voriconazole
- Labeler
- Viona Pharmaceuticals Inc
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20190416
- Source listing expiry
- 20271231
Source-listed ingredients
- VORICONAZOLE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 100 TABLET, FILM COATED in 1 BOTTLE (72578-062-01) · 72578-062-01
- 500 TABLET, FILM COATED in 1 BOTTLE (72578-062-05) · 72578-062-05
- 30 TABLET, FILM COATED in 1 BOTTLE (72578-062-06) · 72578-062-06
- 1000 TABLET, FILM COATED in 1 BOTTLE (72578-062-10) · 72578-062-10
- 90 TABLET, FILM COATED in 1 BOTTLE (72578-062-16) · 72578-062-16
- 10 BLISTER PACK in 1 CARTON (72578-062-77) / 10 TABLET, FILM COATED in 1 BLISTER PACK (72578-062-30) · 72578-062-77
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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