voriconazole
- Product NDC
- 0904-6471
- 11-digit product format
- 009046471
- Labeler code
- 0904
- Product ID
- 0904-6471_0a3b222d-6e9e-4290-9345-fc019279c790
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- voriconazole
- Dosage form
- TABLET, FILM COATED
- Route
- ORAL
- Labeler
- Major Pharmaceuticals
- Application
- ANDA200265
- Marketing category
- ANDA
- Marketing start
- 2015-03-25
- 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
- 2020-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 0904-6471-04 | 00904647104 | 30 BLISTER PACK in 1 CARTON (0904-6471-04) > 1 TABLET, FILM COATED in 1 BLISTER PACK | 30 blister pack | 2015-03-25 | 0000-00-00 | No | No | Current |