Miconazole 3
- Product NDC
- 11673-391
- 11-digit product format
- 116730391
- Labeler code
- 11673
- Product ID
- 11673-391_3a38916c-83b0-dad7-e063-6394a90a8f69
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Miconazole Nitrate
- Dosage form
- CREAM
- Route
- VAGINAL
- Labeler
- TARGET Corporation
- Application
- ANDA076773
- Marketing category
- ANDA
- Marketing start
- 2005-03-02
- Substance
- MICONAZOLE NITRATE
- Active strength
- 40 mg/g
- 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 3
- Listing expiration
- 2026-12-31
Active Ingredients#
Ingredient, Strength table| Ingredient | Strength |
|---|
| MICONAZOLE NITRATE | 40 mg/g |
Harmonized Identifiers#
Field, Values table| Field | Values |
|---|
| Unii | VW4H1CYW1K |
| Rxcui | 998544 |
DailyMed Product Concepts#
DailyMed Package Descriptions#
Package NDC, Product, Description table| Package NDC | Product | Description | Form | Quantity | Strength | SPL version |
|---|
| 11673-391-06 | Miconazole 3 | 25 g in 1 TUBE, WITH APPLICATOR | CREAM | 25 | | 3 |
| 11673-391-06 | Miconazole 3 | 1 in 1 CARTON | CREAM | 1 | | 3 |
DailyMed Dashboard NDC Coverage#
NDC, Dashboard title, SPL version table| NDC | Dashboard title | SPL version | Validation | Dashboard ZIP |
|---|
| 11673-391 | MICONAZOLE 3 (MICONAZOLE NITRATE) CREAM [TARGET CORPORATION] | 2 | Current NDC, Legacy NDC, 2 package rows | 20201211_12a2e441-4fdf-4c5e-b033-ba05ef12fc2f.zip |
DailyMed RxNorm Mappings#
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 11673-391-06 | 11673039106 | 1 TUBE, WITH APPLICATOR in 1 CARTON (11673-391-06) / 25 g in 1 TUBE, WITH APPLICATOR | 2020-10-14 | 0000-00-00 | No | No | Current |