Strength
200 mg/1
Manufacturer
Slate Run Pharmaceuticals LLCNDC
70436002980
Classification
Generic
Dosage Form
INJECTION, POWDER, LYOPHILIZED, FOR SOLUTION
Route
INTRAVENOUS
Last Updated
6/18/2025
Active Ingredients
VORICONAZOLEApproval Type
Generic (ANDA)
FDA Application
ANDA211661On Market Since
1/28/2019
Pharmacological Classes
Azole Antifungal
Azoles
Cytochrome P450 2C19 Inhibitors
Cytochrome P450 2C9 Inhibitors
Cytochrome P450 3A4 Inhibitors
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