Voriconazole
- Product NDC
- 48433-147
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Safecor Health LLC
- Application
- ANDA090547
- Marketing category
- ANDA
- Substance
- VORICONAZOLE
- Current FDA listing
- Yes
Packages
| Package NDC | Description | Marketing start | Marketing end | Sample | Status |
|---|
| 48433-147-03 | 30 BLISTER PACK in 1 CARTON (48433-147-03) / 1 TABLET, FILM COATED in 1 BLISTER PACK (48433-147-01) | 20260406 | | No | Historical |
Related DailyMed Labels
| Set ID | Title | Manufacturer | Effective date | Type | Version |
|---|
| 23f25c6b-f075-42dc-ae05-63b5bf410929 | These highlights do not include all the information needed to use VORICONAZOLE TABLETS safely and effectively. See full prescribing information for VORICONAZOLE TABLETS. VORICONAZOLE tablets, for oral use Initial U.S. Approval: 2002 | Safecor Health LLC | 2026-04-07 | HUMAN PRESCRIPTION DRUG LABEL | 2 |