Fluconazole
- Product NDC
- 63629-1949
- 11-digit product format
- 636291949
- Labeler code
- 63629
- Product ID
- 63629-1949_8b5e84d1-0a5b-4296-a124-874e1e04d1b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluconazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA078423
- Marketing category
- ANDA
- Marketing start
- 2011-03-07
- Marketing end
- 2023-07-31
- Substance
- FLUCONAZOLE
- Active strength
- 200 mg/1
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 2C19 Inhibitors [MoA], Cytochrome P450 2C9 Inhibitors [MoA], Cytochrome P450 3A4 Inhibitors [MoA]
- NDC exclude flag
- No
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| 8VZV102JFY | FLUCONAZOLE | 86386-73-4 | FLUCONAZOLE |
Packages
| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 63629-1949-1 | 63629194901 | 30 TABLET in 1 BOTTLE (63629-1949-1) | 30 tablet | 2021-03-02 | 0000-00-00 | No | No | Current |