FLUCONAZOLE
- Product NDC
- 72189-143
- 11-digit product format
- 721890143
- Labeler code
- 72189
- Product ID
- 72189-143_2becff06-7cc2-1200-e063-6294a90ad1ec
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- FLUCONAZOLE
- Dosage form
- TABLET
- Route
- ORAL
- Labeler
- direct rx
- Application
- ANDA076658
- Marketing category
- ANDA
- Marketing start
- 2020-11-12
- Substance
- FLUCONAZOLE
- Active strength
- 150 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
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- FLUCONAZOLE
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| FLUCONAZOLE | 150 mg/1 |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | 8VZV102JFY |
| Rxcui | 197698, 197699 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 72189-143-01 | FLUCONAZOLE | 1 in 1 DOSE PACK | TABLET | 1 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72189-143 | FLUCONAZOLE TABLET FLUCONAZOLE TABLET [DIRECT RX] | 5 | Current NDC, Legacy NDC, 1 package rows | 20250119_b3db505a-9677-6f5a-e053-2a95a90a13d4.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 72189-143-01 | 72189014301 | 1 TABLET in 1 DOSE PACK (72189-143-01) | 1 tablet | 2020-11-12 | 0000-00-00 | No | No | Current |