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402 402 (Phenytoin Sodium Extended 100 mg)

Pill with imprint 402 402 is White, Capsule-shape and has been identified as Phenytoin Sodium Extended 100 mg. It is supplied by Sun Pharmaceutical Industries Inc..

Phenytoin is used in the treatment of epilepsy; seizures; status epilepticus; seizure prophylaxis during or following neurosurgery; neurosurgery and belongs to the drug classes group I antiarrhythmics, hydantoin anticonvulsants. There is positive evidence of human fetal risk during pregnancy. Phenytoin 100 mg is not a controlled substance under the Controlled Substances Act (CSA).

Images for 402 402

Phenytoin sodium extended 100 mg 402 402 Front
Phenytoin sodium extended 100 mg 402 402 Back

Phenytoin Sodium Extended

Imprint
402 402
Strength
100 mg
Color
White
Size
16.00 mm
Shape
Capsule-shape
Availability
Prescription only
Drug Class
Group i antiarrhythmics, Hydantoin anticonvulsants
Pregnancy Category
D - Positive evidence of risk
CSA Schedule
Not a controlled drug
Labeler / Supplier
Sun Pharmaceutical Industries Inc.
Inactive Ingredients
lactitol monohydrate, sodium lauryl sulfate, magnesium silicate, magnesium stearate, gelatin, ferrosoferric oxide, FD&C Blue No. 2, FD&C Red No. 40, FD&C Blue No. 1, D&C Yellow No. 10, shellac, butyl alcohol, propylene glycol

Note: Inactive ingredients may vary.

Labelers / Repackagers

NDC Code Labeler / Repackager
62756-0402 Sun Pharmaceutical Industries Inc.
54868-5534 Physicians Total Care Inc. (repackager)

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Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.