Ketoconazole 51672-1298
Product NDC
51672-1298- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- December 18, 2002
- Listing Expires
- December 31, 2026
- Application
- ANDA075638
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Ketoconazole | 20 mg/g |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(3)
1 TUBE in 1 CARTON (51672-1298-1) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1298-2) / 30 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1298-3) / 60 g in 1 TUBE