Terbinafine Hydrochloride 51672-2140
Product NDC
51672-2140- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Otc Drug
- Marketing Start
- July 2, 2007
- Listing Expires
- December 31, 2026
- Application
- ANDA077511
Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 1 g/100g |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(1)
1 TUBE in 1 CARTON (51672-2140-1) / 15 g in 1 TUBE