Voriconazole
- Product NDC
- 59762-0930
- 11-digit product format
- 597620930
- Labeler code
- 59762
- Product ID
- 59762-0930_07740108-03ca-49ac-aecb-24a1efa8fd0b
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Greenstone LLC
- Application
- NDA021266
- Marketing category
- NDA AUTHORIZED GENERIC
- Marketing start
- 2010-07-08
- Marketing end
- 0000-00-00
- Substance
- VORICONAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC],Azoles [CS],Cytochrome P450 3A4 Inhibitors [MoA],Cytochrome P450 2C19 Inhibitors [MoA],Cytochrome P450 2C9 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 2021-12-31
- 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 |
|---|
| 59762-0930-2 | 59762093002 | 30 TABLET, FILM COATED in 1 BOTTLE (59762-0930-2) | 2010-07-08 | 0000-00-00 | No | No | Current |