NDCFind

Phenytoin 17856-4070-01

Package NDC

17856-4070-01

Product NDC: 17856-4070

Manufacturer
Atlantic Biologicals Corp.
Dosage Form
Suspension
Route
Oral
Product Type
Human Prescription Drug
Marketing Start
April 8, 2004
Listing Expires
December 31, 2026
Application
ANDA040521
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Active Ingredients

IngredientStrength
Phenytoin125 mg/5mL

Drug Class

Anti-epileptic Agent [EPC]Anti-epileptic Agent [EPC]Cytochrome P450 1A2 Inducers [MoA]

Selected Package

17856-4070-01Selected

72 CUP, UNIT-DOSE in 1 BOX, UNIT-DOSE (17856-4070-1) / 4 mL in 1 CUP, UNIT-DOSE (17856-4070-2)