Terbinafine Hydrochloride 51655-0364
Product NDC
51655-0364- Manufacturer
- Northwind Health Company, Llc
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- May 28, 2020
- Listing Expires
- December 31, 2027
- Application
- ANDA077714
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(1)
90 TABLET in 1 BOTTLE (51655-364-26)