NDA 21464, held by Pfizer. Voriconazole.
As of Nov 14, 2026, NDA 21464 (Vfend), held by Pfizer, was first approved by FDA on Nov 14, 2003, with 0 approved supplements and 0 published complete response letters.
| Date | Submission | Status | Documents |
|---|---|---|---|
| Nov 14, 2003 | Original applicationTYPE 6 · Standard review | Approved |
| Vfend50MG · tablet; oral | Voriconazole | Rx |
| Vfend200MG · tablet; oral | Voriconazole | Rx |
| Vfend200MG · injectable; injection | Voriconazole | Rx |
Approvals, supplements, products and documents come from FDA's Drugs@FDA data files, refreshed daily; Drugs@FDA lists approved applications only. Complete response letters are FDA's published letters. Drugs@FDA and FDA complete response letters