Terbinafine 76282-0209
Product NDC
76282-0209- Manufacturer
- Exelan Pharmaceuticals Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- April 25, 2012
- Listing Expires
- December 31, 2026
- Application
- ANDA077533
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(3)
100 TABLET in 1 BOTTLE (76282-209-01)
500 TABLET in 1 BOTTLE (76282-209-05)
30 TABLET in 1 BOTTLE (76282-209-30)