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
- 27241-063_2de57c37-2e52-4d57-89e9-33a922f9f101
- Product NDC
- 27241-063
- Form
- TABLET, FILM COATED
- Composition / generic term
- Voriconazole
- Labeler
- Ajanta Pharma USA Inc.
- Marketing category
- ANDA
- Marketing start / end (source format)
- 20160531
- Source listing expiry
- 20271231
Source-listed ingredients
- VORICONAZOLE — 200 mg/1
These values do not establish equivalence or a dose recommendation.
Packages
- 30 TABLET, FILM COATED in 1 BOTTLE (27241-063-03) · 27241-063-03
Source and coverage
Open FDA National Drug Code directory →
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.
Browse United States records →