Discontinued
Strength
100 mg/1
Manufacturer
Pfizer Inc.NDC
00071036932
Classification
Brand (ANDA)
Dosage Form
CAPSULE
Route
ORAL
Last Updated
1/1/2026
Active Ingredients
PHENYTOIN SODIUMApproval Type
Generic (ANDA)
FDA Application
ANDA084349On Market Since
8/27/1976
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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