Ketoconazole
- Product NDC
- 71335-2839
- 11-digit product format
- 713352839
- Labeler code
- 71335
- Product ID
- 71335-2839_b6f5f195-1e32-4e50-9414-2d48c13eae5f
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoconazole
- Dosage form
- SHAMPOO, SUSPENSION
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- Application
- ANDA076419
- Marketing category
- ANDA
- Marketing start
- 2010-01-19
- Substance
- KETOCONAZOLE
- Active strength
- 20 mg/mL
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein 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
- Ketoconazole
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| KETOCONAZOLE | 20 mg/mL |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R9400W927I |
| Rxcui | 106336 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 71335-2839-1 | Ketoconazole | 120 mL in 1 BOTTLE | SHAMPOO, SUSPENSION | 120 | | 100 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 71335-2839-1 | 71335283901 | 120 mL in 1 BOTTLE (71335-2839-1) | 120 ml | 2025-10-24 | No | No | Current |