FDA label
What is Dilantin used for?
Dilantin contains phenytoin. The FDA-approved uses below are quoted from the Indications and Usage section of its DailyMed label.
Source: DailyMed SPL label file dated 2026-10-23. Publisher page
The FDA label says: “DILANTIN is indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery.”
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Dilantin, capsule, extended release
Indications and Usage, quoted from the label by Viatris Specialty LLC (ANDA084349). Cross-references to other label sections are left out.
DILANTIN is indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery.
Source: DailyMed label, set id 86dd27d1-9cee-48ae-b55d-e2d2f7dbc593, version 3, effective August 21, 2023. NDC 58151-110, one of 3 listings for this product.
Questions
What is Dilantin used for?
The FDA label says: “DILANTIN is indicated for the treatment of tonic-clonic (grand mal) and psychomotor (temporal lobe) seizures and prevention and treatment of seizures occurring during or following neurosurgery.”
What drug class is Dilantin?
FDA lists phenytoin in the Anti-epileptic Agent established pharmacologic class.
Does this page cover off-label uses or dosing?
No. This page shows only the Indications and Usage section of the FDA label. Ask a pharmacist or prescriber about dosing.
More on Dilantin
- Is Dilantin a controlled substance?Federal schedule
- Generic for DilantinFDA Orange Book
- What is Phenytoin used for?FDA label uses
- Is Phenytoin a controlled substance?Federal schedule
- Generic for Dilantin-125FDA Orange Book
- Anti-epileptic Agents listFDA drug class
- NDC 58151-110Dilantin NDC record
- NDC 58151-118Dilantin NDC record
- NDC 70518-4325Dilantin NDC record