Econazole Nitrate
- Product NDC
- 68788-7406
- 11-digit product format
- 687887406
- Labeler code
- 68788
- Product ID
- 68788-7406_0eae430a-b734-491e-9644-d4758fb40764
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- Econazole Nitrate
- Dosage form
- CREAM
- Route
- TOPICAL
- Labeler
- Preferred Pharmaceuticals Inc.
- Application
- ANDA076574
- Marketing category
- ANDA
- Marketing start
- 2018-06-06
- Marketing end
- 0000-00-00
- Substance
- ECONAZOLE NITRATE
- Active strength
- 10 mg/g
- Pharmacologic classes
- Azole Antifungal [EPC], Azoles [CS]
- NDC exclude flag
- No
- Listing certified through
- 2023-12-31
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 68788-7406-1 | 68788740601 | 15 g in 1 TUBE (68788-7406-1) | 15 g | 2019-09-05 | 0000-00-00 | No | No | Current |
| 68788-7406-3 | 68788740603 | 1 TUBE in 1 CARTON (68788-7406-3) > 30 g in 1 TUBE | 1 tube | 2018-06-06 | 0000-00-00 | No | No | Current |