Voriconazole
- Product NDC
- 27241-062
- 11-digit product format
- 272410062
- Labeler code
- 27241
- Product ID
- 27241-062_2de57c37-2e52-4d57-89e9-33a922f9f101
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Ajanta Pharma USA Inc.
- Application
- ANDA206181
- Marketing category
- ANDA
- Marketing start
- 2016-05-31
- Substance
- VORICONAZOLE
- Active strength
- 50 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 | 50 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | JFU09I87TR |
| Rxcui | 349434, 349435 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 27241-062-03 | Voriconazole | 30 in 1 BOTTLE | TABLET, FILM COATED | 30 | | 22 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 27241-062 | VORICONAZOLE TABLET [AJANTA PHARMA USA INC.] | 20 | Current NDC, Legacy NDC, 1 package rows | 20250417_16a80777-f1f3-45bb-a312-998b07767fe3.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 27241-062-03 | 27241006203 | 30 TABLET, FILM COATED in 1 BOTTLE (27241-062-03) | 2016-05-31 | 0000-00-00 | No | No | Current |