Strength
200 mg/1
Manufacturer
Supernus Pharmaceuticals Inc.NDC
17772013330
Classification
Brand
Dosage Form
CAPSULE, EXTENDED RELEASE
Route
ORAL
Last Updated
1/1/2026
Active Ingredients
VILOXAZINE HYDROCHLORIDEApproval Type
New Drug (NDA)
FDA Application
NDA211964On Market Since
4/2/2021
Pharmacological Classes
Cytochrome P450 1A2 Inhibitors
Cytochrome P450 2B6 Inhibitors
Cytochrome P450 2D6 Inhibitors
Cytochrome P450 3A4 Inhibitors
Norepinephrine Reuptake Inhibitor
Norepinephrine Uptake Inhibitors
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