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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- voriconazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VORICONAZOLE | 200 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JFU09I87TR |
| Rxcui | 349434 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72162-1198-3 | voriconazole | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 100 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1198 | VORICONAZOLE TABLET, FILM COATED [BRYANT RANCH PREPACK] | 100 | Current NDC, 1 package rows | 20250515_35098192-3bcb-9111-e063-6394a90ae8ea.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| 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 | Current |