Voriconazole
- Product NDC
- 39822-1077
- 11-digit product format
- 398221077
- Labeler code
- 39822
- Product ID
- 39822-1077_dc148b7a-01a5-78f6-e053-2a95a90a9b6c
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
- Route
- INTRAVENOUS
- Labeler
- XGen Pharmaceuticals DJB, Inc.
- Application
- NDA208562
- Marketing category
- NDA
- Marketing start
- 2017-03-09
- Marketing end
- 0000-00-00
- Substance
- VORICONAZOLE
- Active strength
- 10 mg/mL
- 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
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 39822-1077-1 | 39822107701 | 1 VIAL, SINGLE-USE in 1 CARTON (39822-1077-1) > 20 mL in 1 VIAL, SINGLE-USE | 2019-06-14 | 0000-00-00 | No | No | Current |