Terbinafine Hydrochloride 51672-2080
Product NDC
51672-2080- Manufacturer
- Sun Pharmaceutical Industries, Inc.
- Dosage Form
- Cream
- Route
- Topical
- Product Type
- Human Otc Drug
- Marketing Start
- July 2, 2007
- Listing Expires
- December 31, 2027
- Application
- ANDA077511
Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 1 g/100g |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(7)
1 TUBE in 1 CARTON (51672-2080-1) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-2) / 30 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-3) / 60 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-4) / 15 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-6) / 45 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-8) / 12 g in 1 TUBE
1 TUBE in 1 CARTON (51672-2080-9) / 24 g in 1 TUBE