Voriconazole
- Product NDC
- 55801-332
- 11-digit product format
- 558010332
- Labeler code
- 55801
- Product ID
- 55801-332_b87b650c-9a4b-4c82-975e-f62d12f20487
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Voriconazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- APPCO PHARMA LLC
- Application
- ANDA206762
- Marketing category
- ANDA
- Marketing start
- 2016-05-26
- 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
- 2019-12-31
- Current FDA listing
- Historical FDA.report record