voriconazole
- Product NDC
- 64980-274
- 11-digit product format
- 649800274
- Labeler code
- 64980
- Product ID
- 64980-274_da3e4690-b6ba-4922-9d44-f435add1eb35
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Rising Pharmaceuticals, Inc.
- Application
- ANDA206762
- Marketing category
- ANDA
- Marketing start
- 2016-12-07
- Marketing end
- 0000-00-00
- Substance
- VORICONAZOLE
- Active strength
- 50 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
- 2020-12-31
- 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 |
|---|
| 64980-274-03 | 64980027403 | 30 TABLET, FILM COATED in 1 BOTTLE (64980-274-03) | 2016-12-07 | 0000-00-00 | No | No | Current |