Voriconazole
- Product NDC
- 0904-7024
- 11-digit product format
- 009047024
- Labeler code
- 0904
- Product ID
- 0904-7024_5a20ebfc-ed32-437c-bb18-40cdbc991131
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA206181
- Marketing category
- ANDA
- Marketing start
- 2016-05-31
- 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
- 2027-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Voriconazole
- Listing expiration
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| VORICONAZOLE | 200 mg/1 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 0904-7024-04 | Voriconazole | 1 in 1 BLISTER PACK | TABLET, FILM COATED | 1 | | 7 |
| 0904-7024-04 | Voriconazole | 30 in 1 CARTON | TABLET, FILM COATED | 30 | | 7 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 0904-7024 | VORICONAZOLE TABLET [MAJOR PHARMACEUTICALS] | 4 | Current NDC, Legacy NDC, 2 package rows | 20250110_796cad15-2aef-4823-917d-17b822a6916e.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-7024-04 | 00904702404 | 30 BLISTER PACK in 1 CARTON (0904-7024-04) / 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2016-05-31 | 0000-00-00 | No | No | Current |