Econazole Nitrate
- Product NDC
- 68788-8884
- 11-digit product format
- 687888884
- Labeler code
- 68788
- Product ID
- 68788-8884_2bd2a48e-cbef-4b14-a02f-9aa693cc4b47
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Econazole Nitrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076479
- Marketing category
- ANDA
- Marketing start
- 2006-08-08
- Substance
- ECONAZOLE NITRATE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes
Additional Listing Data#
- Finished product
- Yes
- Brand name base
- Econazole Nitrate
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ECONAZOLE NITRATE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H438WYN10E |
| Rxcui | 857366 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 68788-8884-3 | Econazole Nitrate | 30 g in 1 TUBE | CREAM | 30 | | 1 |
| 68788-8884-3 | Econazole Nitrate | 1 in 1 CARTON | CREAM | 1 | | 1 |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Sample | Exclude flag | Status |
|---|
| 68788-8884-3 | 68788888403 | 1 TUBE in 1 CARTON (68788-8884-3) / 30 g in 1 TUBE | 1 tube | 2025-06-02 | No | No | Historical |