Terbinafine 72189-0243
Product NDC
72189-0243- Manufacturer
- Direct Rx
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- July 23, 2021
- Listing Expires
- December 31, 2026
- Application
- ANDA078297
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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 (72189-243-30)