Miconazole Nitrate 51672-2035
Product NDC
51672-2035- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Vaginal
- Product Type
- Human Otc Drug
- Marketing Start
- January 13, 1997
- Listing Expires
- December 31, 2026
- Application
- ANDA074444
Active Ingredients
| Ingredient | Strength |
|---|---|
| Miconazole Nitrate | 20 mg/g |
Drug Class
Azole Antifungal [EPC]Azoles [CS]
Packaging Options(2)
1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2035-6) / 45 g in 1 TUBE, WITH APPLICATOR
1 TUBE, WITH APPLICATOR in 1 CARTON (51672-2035-7) / 45 g in 1 TUBE, WITH APPLICATOR