ECOZA
- Product NDC
- 23710-100
- 11-digit product format
- 237100100
- Labeler code
- 23710
- Product ID
- 23710-100_d488dcc9-a064-2814-e053-2995a90ac26a
- Type
- HUMAN PRESCRIPTION DRUG
- Nonproprietary name
- econazole nitrate
- Dosage form
- AEROSOL, FOAM
- Route
- TOPICAL
- Labeler
- Exeltis USA Dermatology, LLC
- Application
- NDA205175
- Marketing category
- NDA
- Marketing start
- 2020-10-02
- 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 |
|---|
| 23710-100-70 | 23710010070 | 1 CANISTER in 1 CARTON (23710-100-70) > 70 g in 1 CANISTER | 1 canister | 2020-10-02 | 0000-00-00 | No | No | Current |