voriconazole
- Product NDC
- 72162-1198
- 11-digit product format
- 721621198
- Labeler code
- 72162
- Product ID
- 72162-1198_350989fb-8ab1-94a3-e063-6394a90a1a9a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA200265
- Marketing category
- ANDA
- Marketing start
- 2025-05-13
- Substance
- VORICONAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| JFU09I87TR | VORICONAZOLE | 137234-62-9 | VORICONAZOLE |
Packages
| Package NDC | 11-digit format | Description | Marketing start | Sample | Exclude flag | Status |
|---|
| 72162-1198-3 | 72162119803 | 30 TABLET, FILM COATED in 1 BOTTLE (72162-1198-3) | 2025-05-13 | No | No | Historical |
Related DailyMed Labels
| Title | Manufacturer | Effective date | Type | Version |
|---|
| voriconazole | Bryant Ranch Prepack | 2025-05-13 | HUMAN PRESCRIPTION DRUG LABEL | 100 |