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
Related UNII Ingredients
| UNII | Preferred term | Registry number | Matched term |
|---|
| H438WYN10E | ECONAZOLE NITRATE | 24169-02-6 | ECONAZOLE NITRATE |
Packages
| 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 | Historical |
| 72162-1410-3 | 72162141003 | 1 TUBE in 1 CARTON (72162-1410-3) / 30 g in 1 TUBE | 1 tube | 2023-08-17 | No | No | Historical |
| 72162-1410-4 | 72162141004 | 1 TUBE in 1 CARTON (72162-1410-4) / 15 g in 1 TUBE | 1 tube | 2023-08-17 | No | No | Historical |