Strength
25 mg/mL
Manufacturer
Azurity Pharmaceuticals Inc.NDC
52652900101
Classification
Brand
Dosage Form
SOLUTION
Route
ORAL
Last Updated
1/1/2026
Active Ingredients
TOPIRAMATEApproval Type
New Drug (NDA)
FDA Application
NDA214679On Market Since
12/6/2021
Pharmacological Classes
Cytochrome P450 2C19 Inhibitors
Cytochrome P450 3A4 Inducers
Decreased Central Nervous System Disorganized Electrical Activity
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