Miconazole Nitrate Antifungal Powder
- Product NDC
- 10135-720
- 11-digit product format
- 101350720
- Labeler code
- 10135
- Product ID
- 10135-720_441cab8b-3a58-00e0-e063-6294a90aaa23
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate Antifungal Powder
- Dosage form
- POWDER
- Route
- TOPICAL
- Labeler
- Marlex Pharmaceuticals, Inc.
- Application
- M005
- Marketing category
- OTC MONOGRAPH DRUG
- Marketing start
- 2022-05-01
- Substance
- MICONAZOLE NITRATE
- Active strength
- 2 g/100g
- 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
- Miconazole Nitrate Antifungal Powder
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 2 g/100g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998461 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 10135-720-85 | Miconazole Nitrate Antifungal Powder | 85 g in 1 BOTTLE | POWDER | 85 | | 4 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 10135-720 | MICONAZOLE NITRATE ANTIFUNGAL POWDER POWDER [MARLEX PHARMACEUTICALS, INC.] | 3 | Current NDC, Legacy NDC, 1 package rows | 20241016_de4f703c-39e9-855e-e053-2a95a90a6ea9.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 10135-720-85 | 10135072085 | 85 g in 1 BOTTLE (10135-720-85) | 85 g | 2022-05-01 | 0000-00-00 | No | No | Current |