Terbinafine Hydrochloride 69452-0351
Product NDC
69452-0351- Manufacturer
- Bionpharma Inc.
- Dosage Form
- Tablet
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- January 28, 2022
- Listing Expires
- December 31, 2026
- Application
- ANDA078163
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Terbinafine Hydrochloride | 250 mg/1 |
Drug Class
Allylamine Antifungal [EPC]Allylamine [CS]
Packaging Options(2)
30 TABLET in 1 BOTTLE, PLASTIC (69452-351-13)
100 TABLET in 1 BOTTLE, PLASTIC (69452-351-20)