Miconazole Nitrate 51672-2070
Product NDC
51672-2070- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Vaginal
- Product Type
- Human Otc Drug
- Marketing Start
- March 2, 2005
- Listing Expires
- December 31, 2026
- Application
- ANDA076773
Active Ingredients
| Ingredient | Strength |
|---|---|
| Miconazole Nitrate | 40 mg/g |
Drug Class
Azole Antifungal [EPC]Azoles [CS]
Packaging Options(1)
1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2070-9) / 25 g in 1 TUBE, WITH APPLICATOR