Low Outlier
Strength
125 mg/5mL
Manufacturer
Sun Pharmaceutical Industries Inc.NDC
51672406901
Classification
Generic
Dosage Form
SUSPENSION
Route
ORAL
Last Updated
4/22/2026
Active Ingredients
PHENYTOINApproval Type
Generic (ANDA)
FDA Application
ANDA040521On Market Since
4/8/2004
Pharmacological Classes
Anti-epileptic Agent
Cytochrome P450 1A2 Inducers
Cytochrome P450 2B6 Inducers
Cytochrome P450 2C19 Inducers
Cytochrome P450 2C8 Inducers
Cytochrome P450 2C9 Inducers
Cytochrome P450 2D6 Inducers
Cytochrome P450 3A Inducers
Decreased Central Nervous System Disorganized Electrical Activity
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