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
- 68462-573_1c47b796-6b3e-4321-86f6-f51fbf9a39fb
- Product NDC
- 68462-573
- Form
- TABLET, FILM COATED
- Composition / generic term
- voriconazole
- Labeler
- Glenmark Pharmaceuticals Inc., USA
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20150904 / 20270101
Source-listed ingredients
- VORICONAZOLE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 3 BLISTER PACK in 1 CARTON (68462-573-13) / 10 TABLET, FILM COATED in 1 BLISTER PACK · 68462-573-13
- 30 TABLET, FILM COATED in 1 BOTTLE (68462-573-30) · 68462-573-30
- 90 TABLET, FILM COATED in 1 BOTTLE (68462-573-90) · 68462-573-90
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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