Voriconazole
- Product NDC
- 61748-366
- 11-digit product format
- 617480366
- Labeler code
- 61748
- Product ID
- 61748-366_4939f180-1541-4143-81a7-a281bfbd01ed
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- VersaPharm Incorporated
- Application
- ANDA207049
- Marketing category
- ANDA
- Marketing start
- 2016-09-07
- 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 |
|---|
| 61748-366-30 | 61748036630 | 30 TABLET, FILM COATED in 1 BOTTLE, PLASTIC (61748-366-30) | 2016-09-07 | 0000-00-00 | No | No | Current |