Terbinafine Hydrochloride 68071-1640
Product NDC
68071-1640- Manufacturer
- Nucare Pharmaceuticals,inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- August 13, 2014
- Listing Expires
- December 31, 2026
- Application
- ANDA077137
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(1)
30 TABLET in 1 BOTTLE (68071-1640-3)