Micotrin AP
- Product NDC
- 59088-478
- 11-digit product format
- 590880478
- Labeler code
- 59088
- Product ID
- 59088-478_23737640-ab36-eddf-e063-6394a90a3bef
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- PureTek Corporation
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2021-10-25
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 g/85g
- 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
- Micotrin AP
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 2 g/85g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 59088-478-07 | Micotrin AP | 85 g in 1 BOTTLE | POWDER | 85 | | 5 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 59088-478 | MICOTRIN AP (MICONAZOLE NITRATE) POWDER [PURETEK CORPORATION] | 5 | Current NDC, Legacy NDC, 1 package rows | 20241004_cbe3d495-cdee-2343-e053-2a95a90a5b82.zip |
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 59088-478-07 | 59088047807 | 85 g in 1 BOTTLE (59088-478-07) | 85 g | 2021-10-25 | 0000-00-00 | No | No | Current |