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
- 16714-198_45de5a3f-4e1f-4870-b4aa-3057e4e2ba7f
- Product NDC
- 16714-198
- Form
- TABLET, FILM COATED
- Composition / generic term
- Voriconazole
- Labeler
- NorthStar Rx LLC
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160122 / 20270430
Source-listed ingredients
- VORICONAZOLE — 50 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (16714-198-01) · 16714-198-01
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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