Naftifine Hydrochloride 51672-1376-03
- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Gel
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- April 1, 2023
- Listing Expires
- December 31, 2027
- Application
- ANDA208201
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Naftifine Hydrochloride | 20 mg/g |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Selected Package
51672-1376-03Selected1 TUBE in 1 CARTON (51672-1376-3) / 60 g in 1 TUBE
Other packages for this product(1)
1 TUBE in 1 CARTON (51672-1376-6) / 45 g in 1 TUBE