Fluconazole
- Product NDC
- 82804-030
- 11-digit product format
- 828040030
- Labeler code
- 82804
- Product ID
- 82804-030_fc4fccd8-19d2-4704-afa9-9ce0ab1d2b5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Fluconazole
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- Proficient Rx LP
- Application
- ANDA077731
- Marketing category
- ANDA
- Marketing start
- 2008-10-07
- 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
- 2026-12-31
- Current FDA listing
- Yes
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 | Sample | Exclude flag | Status |
|---|
| 82804-030-30 | 82804003030 | 30 TABLET in 1 BOTTLE (82804-030-30) | 30 tablet | 2023-10-20 | No | No | Historical |
| 82804-030-60 | 82804003060 | 60 TABLET in 1 BOTTLE (82804-030-60) | 60 tablet | 2023-10-20 | No | No | Historical |
| 82804-030-90 | 82804003090 | 90 TABLET in 1 BOTTLE (82804-030-90) | 90 tablet | 2023-10-20 | No | No | Historical |