Ketoconazole
- Product NDC
- 70518-4236
- 11-digit product format
- 705184236
- Labeler code
- 70518
- Product ID
- 70518-4236_4006996a-6889-c723-e063-6394a90abc17
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Ketoconazole Cream, 2%
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- REMEDYREPACK INC.
- Application
- ANDA212443
- Marketing category
- ANDA
- Marketing start
- 2024-12-05
- Substance
- KETOCONAZOLE
- Active strength
- 20 mg/g
- 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/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | R9400W927I |
| Rxcui | 203088 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 70518-4236-0 | Ketoconazole | 30 g in 1 TUBE | CREAM | 30 | | 3 |
| 70518-4236-0 | Ketoconazole | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 70518-4236 | KETOCONAZOLE (KETOCONAZOLE CREAM, 2%) CREAM [REMEDYREPACK INC.] | 1 | Current NDC, 2 package rows | 20241213_ea56cddf-94c9-46b6-8791-995b741cfbd7.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 70518-4236-0 | 70518423600 | 1 TUBE in 1 CARTON (70518-4236-0) / 30 g in 1 TUBE | 1 tube | 2024-12-05 | No | No | Current |