Tavaborole 70771-1826
Product NDC
70771-1826- Manufacturer
- Zydus Lifesciences Limited
- Dosage Form
- Solution
- Route
- Topical
- Product Type
- Human Prescription Drug
- Marketing Start
- April 24, 2023
- Listing Expires
- December 31, 2026
- Application
- ANDA212294
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Tavaborole | 43.5 mg/mL |
Drug Class
Oxaborole Antifungal [EPC]Boron Compounds [CS]Oxaborole Antifungal [EPC]
Packaging Options(1)
1 BOTTLE, WITH APPLICATOR in 1 CARTON (70771-1826-0) / 10 mL in 1 BOTTLE, WITH APPLICATOR