Naftifine Hydrochloride 51672-1362
Product NDC
51672-1362- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- September 8, 2016
- Listing Expires
- December 31, 2026
- Application
- ANDA205975
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naftifine Hydrochloride | 10 mg/g |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(4)
1 TUBE in 1 CARTON (51672-1362-1) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1362-2) / 30 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1362-3) / 60 g in 1 TUBE
1 TUBE in 1 CARTON (51672-1362-8) / 90 g in 1 TUBE