Voriconazole 70436-0029
Product NDC
70436-0029- Manufacturer
- Slate Run Pharmaceuticals
- Dosage Form
- Injection, Powder, Lyophilized, For Solution
- Route
- Intravenous
- Product Type
- Human Prescription Drug
- Marketing Start
- January 28, 2019
- Listing Expires
- December 31, 2027
- Application
- ANDA211661
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Active Ingredients
| Ingredient | Strength |
|---|---|
| Voriconazole | 200 mg/1 |
Drug Class
Azole Antifungal [EPC]Azole Antifungal [EPC]Azoles [CS]
Packaging Options(1)
1 INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION in 1 BOX (70436-029-80)