Econazole Nitrate
- Product NDC
- 72162-1410
- 11-digit product format
- 721621410
- Labeler code
- 72162
- Product ID
- 72162-1410_e21cc7c8-d197-493b-83fb-6a530771c2b7
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Econazole Nitrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Bryant Ranch Prepack
- 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
- 2027-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| ECONAZOLE NITRATE | 10 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | H438WYN10E |
DailyMed Product Concepts#
DailyMed Package Descriptions#
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 72162-1410 | ECONAZOLE NITRATE CREAM [BRYANT RANCH PREPACK] | 101 | Current NDC, 6 package rows | 20240315_790a86cc-e93b-4bb6-9b60-08b2c4587081.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 |
|---|
| 72162-1410-2 | 72162141002 | 1 TUBE in 1 CARTON (72162-1410-2) / 85 g in 1 TUBE | 1 tube | 2023-08-17 | No | No | Current |
| 72162-1410-3 | 72162141003 | 1 TUBE in 1 CARTON (72162-1410-3) / 30 g in 1 TUBE | 1 tube | 2023-08-17 | No | No | Current |
| 72162-1410-4 | 72162141004 | 1 TUBE in 1 CARTON (72162-1410-4) / 15 g in 1 TUBE | 1 tube | 2023-08-17 | No | No | Current |