Voriconazole 70436-0230
Product NDC
70436-0230- Manufacturer
- Slate Run Pharmaceuticals, Llc
- Dosage Form
- Powder, For Suspension
- Route
- Oral
- Product Type
- Human Prescription Drug
- Marketing Start
- March 1, 2024
- Listing Expires
- December 31, 2026
- Application
- ANDA216805
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Voriconazole | 40 mg/mL |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(1)
1 BOTTLE in 1 CARTON (70436-230-39) / 75 mL in 1 BOTTLE